Canonical Allele Identifier: CA242471478

Gene: PAH

Linked Data

• dbSNP Id: rs145709393
• gnomAD v3: 12-102852723-C-G
• gnomAD v4: 12-102852723-C-G
• MyVariant Identifiers: chr12:g.103246501C>G (hg19) ; chr12:g.102852723C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852723C>G , CM000674.2:g.102852723C>G	GRCh38
NC_000012.11:g.103246501C>G , CM000674.1:g.103246501C>G	GRCh37
NC_000012.10:g.101770631C>G	NCBI36
NG_008690.1:g.69880G>C
NG_008690.2:g.110688G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.842+92G>C MANE Select	ENSP00000448059.1:n.842+92G>C
ENST00000307000.7:c.827+92G>C	ENSP00000303500.2:n.827+92G>C
ENST00000549247.6:n.601+92G>C
ENST00000553106.5:c.842+92G>C	ENSP00000448059.1:n.842+92G>C
ENST00000635477.1:c.3+92G>C
NM_000277.1:c.842+92G>C	NP_000268.1:n.842+92G>C
XM_011538422.1:c.842+92G>C	XP_011536724.1:n.842+92G>C
NM_000277.2:c.842+92G>C	NP_000268.1:n.842+92G>C
NM_001354304.1:c.842+92G>C	NP_001341233.1:n.842+92G>C
NM_000277.3:c.842+92G>C MANE Select	NP_000268.1:n.842+92G>C
NM_001354304.2:c.842+92G>C	NP_001341233.1:n.842+92G>C