Canonical Allele Identifier: CA682819242
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1228656423

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917324G>A , CM000674.2:g.102917324G>A GRCh38
NC_000012.11:g.103311102G>A , CM000674.1:g.103311102G>A GRCh37
NC_000012.10:g.101835232G>A NCBI36
NG_008690.1:g.5280C>T
NG_008690.2:g.46087C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000546708.5:n.493-99C>T
ENST00000546844.1:c.-95-99C>T ENSP00000446658.1:n.-95-99C>T
ENST00000547319.1:n.217-99C>T
ENST00000551337.5:c.-95-99C>T ENSP00000447620.1:n.-95-99C>T
ENST00000553106.5:c.-194C>T ENSP00000448059.1:n.-194C>T
ENST00000635500.1:n.29-4426C>T
NM_000277.1:c.-193C>T NP_000268.1:n.-193C>T
NM_000277.2:c.-194C>T NP_000268.1:n.-194C>T
NM_001354304.1:c.-95-99C>T NP_001341233.1:n.-95-99C>T
NM_001354304.2:c.-95-99C>T NP_001341233.1:n.-95-99C>T