Canonical Allele Identifier: CA2059445950
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1875215664
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852808T>A , CM000674.2:g.102852808T>A GRCh38
NC_000012.11:g.103246586T>A , CM000674.1:g.103246586T>A GRCh37
NC_000012.10:g.101770716T>A NCBI36
NG_008690.1:g.69795A>T
NG_008690.2:g.110603A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.842+7A>T MANE Select ENSP00000448059.1:n.842+7A>T
ENST00000307000.7:c.827+7A>T ENSP00000303500.2:n.827+7A>T
ENST00000549247.6:n.601+7A>T
ENST00000553106.5:c.842+7A>T ENSP00000448059.1:n.842+7A>T
ENST00000635477.1:c.3+7A>T
NM_000277.1:c.842+7A>T NP_000268.1:n.842+7A>T
XM_011538422.1:c.842+7A>T XP_011536724.1:n.842+7A>T
NM_000277.2:c.842+7A>T NP_000268.1:n.842+7A>T
NM_001354304.1:c.842+7A>T NP_001341233.1:n.842+7A>T
NM_000277.3:c.842+7A>T MANE Select NP_000268.1:n.842+7A>T
NM_001354304.2:c.842+7A>T NP_001341233.1:n.842+7A>T
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