Canonical Allele Identifier: CA386295623
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103246674A>T (hg19) chr12:g.102852896A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852896A>T , CM000674.2:g.102852896A>T GRCh38
NC_000012.11:g.103246674A>T , CM000674.1:g.103246674A>T GRCh37
NC_000012.10:g.101770804A>T NCBI36
NG_008690.1:g.69707T>A
NG_008690.2:g.110515T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.761T>A MANE Select ENSP00000448059.1:p.Phe254Tyr
ENST00000307000.7:c.746T>A ENSP00000303500.2:p.Phe249Tyr
ENST00000549247.6:n.520T>A
ENST00000553106.5:c.761T>A ENSP00000448059.1:p.Phe254Tyr
NM_000277.1:c.761T>A NP_000268.1:p.Phe254Tyr
XM_011538422.1:c.761T>A XP_011536724.1:p.Phe254Tyr
NM_000277.2:c.761T>A NP_000268.1:p.Phe254Tyr
NM_001354304.1:c.761T>A NP_001341233.1:p.Phe254Tyr
NM_000277.3:c.761T>A MANE Select NP_000268.1:p.Phe254Tyr
NM_001354304.2:c.761T>A NP_001341233.1:p.Phe254Tyr
Search 100 bp 5'
Search 100 bp 3'