Canonical Allele Identifier: CA386302362
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs2136728171
MyVariant Identifiers: chr12:g.103306600C>A (hg19) chr12:g.102912822C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102912822C>A , CM000674.2:g.102912822C>A GRCh38
NC_000012.11:g.103306600C>A , CM000674.1:g.103306600C>A GRCh37
NC_000012.10:g.101830730C>A NCBI36
NG_008690.1:g.9781G>T
NG_008690.2:g.50589G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.137G>T MANE Select ENSP00000448059.1:p.Gly46Val
ENST00000307000.7:c.122G>T ENSP00000303500.2:p.Gly41Val
ENST00000546844.1:c.137G>T ENSP00000446658.1:p.Gly46Val
ENST00000548677.2:n.224G>T
ENST00000548928.1:n.59G>T
ENST00000549111.5:n.233G>T
ENST00000550978.6:c.121G>T
ENST00000551337.5:c.137G>T ENSP00000447620.1:p.Gly46Val
ENST00000551988.5:n.226G>T
ENST00000553106.5:c.137G>T ENSP00000448059.1:p.Gly46Val
ENST00000635500.1:n.105G>T
NM_000277.1:c.137G>T NP_000268.1:p.Gly46Val
XM_011538422.1:c.137G>T XP_011536724.1:p.Gly46Val
NM_000277.2:c.137G>T NP_000268.1:p.Gly46Val
NM_001354304.1:c.137G>T NP_001341233.1:p.Gly46Val
XM_017019370.2:c.137G>T XP_016874859.1:p.Gly46Val
NM_000277.3:c.137G>T MANE Select NP_000268.1:p.Gly46Val
NM_001354304.2:c.137G>T NP_001341233.1:p.Gly46Val
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