Canonical Allele Identifier: CA229688
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102781
ClinVar RCV Id: RCV000089032
dbSNP Id: rs62517204

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855168G>C , CM000674.2:g.102855168G>C GRCh38
NC_000012.11:g.103248946G>C , CM000674.1:g.103248946G>C GRCh37
NC_000012.10:g.101773076G>C NCBI36
NG_008690.1:g.67435C>G
NG_008690.2:g.108243C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.674C>G MANE Select ENSP00000448059.1:p.Pro225Arg
ENST00000307000.7:c.659C>G ENSP00000303500.2:p.Pro220Arg
ENST00000549111.5:n.770C>G
ENST00000553106.5:c.674C>G ENSP00000448059.1:p.Pro225Arg
NM_000277.1:c.674C>G NP_000268.1:p.Pro225Arg
XM_011538422.1:c.674C>G XP_011536724.1:p.Pro225Arg
NM_000277.2:c.674C>G NP_000268.1:p.Pro225Arg
NM_001354304.1:c.674C>G NP_001341233.1:p.Pro225Arg
XM_017019370.2:c.674C>G XP_016874859.1:p.Pro225Arg
NM_000277.3:c.674C>G MANE Select NP_000268.1:p.Pro225Arg
NM_001354304.2:c.674C>G NP_001341233.1:p.Pro225Arg