Canonical Allele Identifier: CA481578586
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103249050C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855272C>A , CM000674.2:g.102855272C>A GRCh38
NC_000012.11:g.103249050C>A , CM000674.1:g.103249050C>A GRCh37
NC_000012.10:g.101773180C>A NCBI36
NG_008690.1:g.67331G>T
NG_008690.2:g.108139G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.570G>T MANE Select ENSP00000448059.1:p.Val190=
ENST00000307000.7:c.555G>T ENSP00000303500.2:p.Val185=
ENST00000549111.5:n.666G>T
ENST00000553106.5:c.570G>T ENSP00000448059.1:p.Val190=
NM_000277.1:c.570G>T NP_000268.1:p.Val190=
XM_011538422.1:c.570G>T XP_011536724.1:p.Val190=
NM_000277.2:c.570G>T NP_000268.1:p.Val190=
NM_001354304.1:c.570G>T NP_001341233.1:p.Val190=
XM_017019370.2:c.570G>T XP_016874859.1:p.Val190=
NM_000277.3:c.570G>T MANE Select NP_000268.1:p.Val190=
NM_001354304.2:c.570G>T NP_001341233.1:p.Val190=
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