Canonical Allele Identifier: CA481332680
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 755953
ClinVar RCV Id: RCV000933420
dbSNP Id: rs1592968741
MyVariant Identifiers: chr12:g.103271267A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877489A>G , CM000674.2:g.102877489A>G GRCh38
NC_000012.11:g.103271267A>G , CM000674.1:g.103271267A>G GRCh37
NC_000012.10:g.101795397A>G NCBI36
NG_008690.1:g.45114T>C
NG_008690.2:g.85922T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.414T>C MANE Select ENSP00000448059.1:p.Tyr138=
ENST00000307000.7:c.399T>C ENSP00000303500.2:p.Tyr133=
ENST00000549111.5:n.510T>C
ENST00000550978.6:c.398T>C
ENST00000551988.5:n.503T>C
ENST00000553106.5:c.414T>C ENSP00000448059.1:p.Tyr138=
NM_000277.1:c.414T>C NP_000268.1:p.Tyr138=
XM_011538422.1:c.414T>C XP_011536724.1:p.Tyr138=
NM_000277.2:c.414T>C NP_000268.1:p.Tyr138=
NM_001354304.1:c.414T>C NP_001341233.1:p.Tyr138=
XM_017019370.2:c.414T>C XP_016874859.1:p.Tyr138=
NM_000277.3:c.414T>C MANE Select NP_000268.1:p.Tyr138=
NM_001354304.2:c.414T>C NP_001341233.1:p.Tyr138=