Canonical Allele Identifier: CA951260950
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1878425760

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917311G>T , CM000674.2:g.102917311G>T GRCh38
NC_000012.11:g.103311089G>T , CM000674.1:g.103311089G>T GRCh37
NC_000012.10:g.101835219G>T NCBI36
NG_008690.1:g.5293C>A
NG_008690.2:g.46100C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-86C>A
ENST00000546844.1:c.-95-86C>A ENSP00000446658.1:n.-95-86C>A
ENST00000547319.1:n.217-86C>A
ENST00000551337.5:c.-95-86C>A ENSP00000447620.1:n.-95-86C>A
ENST00000553106.5:c.-181C>A ENSP00000448059.1:n.-181C>A
ENST00000635500.1:n.29-4413C>A
NM_000277.1:c.-180C>A NP_000268.1:n.-180C>A
NM_000277.2:c.-181C>A NP_000268.1:n.-181C>A
NM_001354304.1:c.-95-86C>A NP_001341233.1:n.-95-86C>A
NM_001354304.2:c.-95-86C>A NP_001341233.1:n.-95-86C>A