Canonical Allele Identifier: CA386304278
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102894920-T-A
MyVariant Identifiers: chr12:g.103288698T>A (hg19) chr12:g.102894920T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894920T>A , CM000674.2:g.102894920T>A GRCh38
NC_000012.11:g.103288698T>A , CM000674.1:g.103288698T>A GRCh37
NC_000012.10:g.101812828T>A NCBI36
NG_008690.1:g.27683A>T
NG_008690.2:g.68491A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.169-2A>T MANE Select ENSP00000448059.1:n.169-2A>T
ENST00000307000.7:c.154-2A>T ENSP00000303500.2:n.154-2A>T
ENST00000546844.1:c.169-2A>T ENSP00000446658.1:n.169-2A>T
ENST00000548677.2:n.256-2A>T
ENST00000548928.1:n.91-2A>T
ENST00000549111.5:n.265-2A>T
ENST00000550978.6:c.153-2A>T
ENST00000551337.5:c.169-2A>T ENSP00000447620.1:n.169-2A>T
ENST00000551988.5:n.258-2A>T
ENST00000553106.5:c.169-2A>T ENSP00000448059.1:n.169-2A>T
ENST00000635500.1:n.137-2A>T
NM_000277.1:c.169-2A>T NP_000268.1:n.169-2A>T
XM_011538422.1:c.169-2A>T XP_011536724.1:n.169-2A>T
NM_000277.2:c.169-2A>T NP_000268.1:n.169-2A>T
NM_001354304.1:c.169-2A>T NP_001341233.1:n.169-2A>T
XM_017019370.2:c.169-2A>T XP_016874859.1:n.169-2A>T
NM_000277.3:c.169-2A>T MANE Select NP_000268.1:n.169-2A>T
NM_001354304.2:c.169-2A>T NP_001341233.1:n.169-2A>T
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