Canonical Allele Identifier: CA2726766272
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1874723355
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844168C>T , CM000674.2:g.102844168C>T GRCh38
NC_000012.11:g.103237946C>T , CM000674.1:g.103237946C>T GRCh37
NC_000012.10:g.101762076C>T NCBI36
NG_008690.1:g.78435G>A
NG_008690.2:g.119243G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1065+168G>A MANE Select ENSP00000448059.1:n.1065+168G>A
ENST00000307000.7:c.1050+168G>A ENSP00000303500.2:n.1050+168G>A
ENST00000549247.6:n.824+168G>A
ENST00000551114.2:n.727+168G>A
ENST00000553106.5:c.1065+168G>A ENSP00000448059.1:n.1065+168G>A
ENST00000635477.1:c.169+168G>A
ENST00000635528.1:n.580+168G>A
NM_000277.1:c.1065+168G>A NP_000268.1:n.1065+168G>A
XM_011538422.1:c.1008+168G>A XP_011536724.1:n.1008+168G>A
NM_000277.2:c.1065+168G>A NP_000268.1:n.1065+168G>A
NM_001354304.1:c.1065+168G>A NP_001341233.1:n.1065+168G>A
NM_000277.3:c.1065+168G>A MANE Select NP_000268.1:n.1065+168G>A
NM_001354304.2:c.1065+168G>A NP_001341233.1:n.1065+168G>A
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