Canonical Allele Identifier: CA229704
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102794
dbSNP Id: rs62514938

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852952T>C , CM000674.2:g.102852952T>C GRCh38
NC_000012.11:g.103246730T>C , CM000674.1:g.103246730T>C GRCh37
NC_000012.10:g.101770860T>C NCBI36
NG_008690.1:g.69651A>G
NG_008690.2:g.110459A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.707-2A>G MANE Select ENSP00000448059.1:n.707-2A>G
ENST00000307000.7:c.692-2A>G ENSP00000303500.2:n.692-2A>G
ENST00000549247.6:n.464A>G
ENST00000553106.5:c.707-2A>G ENSP00000448059.1:n.707-2A>G
NM_000277.1:c.707-2A>G NP_000268.1:n.707-2A>G
XM_011538422.1:c.707-2A>G XP_011536724.1:n.707-2A>G
NM_000277.2:c.707-2A>G NP_000268.1:n.707-2A>G
NM_001354304.1:c.707-2A>G NP_001341233.1:n.707-2A>G
NM_000277.3:c.707-2A>G MANE Select NP_000268.1:n.707-2A>G
NM_001354304.2:c.707-2A>G NP_001341233.1:n.707-2A>G