Canonical Allele Identifier: CA2681069848

Gene: SLC22A2

Linked Data

• gnomAD v4: 6-160249106-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160249106A>G , CM000668.2:g.160249106A>G	GRCh38
NC_000006.11:g.160670138A>G , CM000668.1:g.160670138A>G	GRCh37
NC_000006.10:g.160590128A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366953.8:c.842+110T>C MANE Select	ENSP00000355920.3:n.842+110T>C
ENST00000366952.1:c.779+110T>C	ENSP00000355919.1:n.779+110T>C
ENST00000366953.7:c.842+110T>C	ENSP00000355920.3:n.842+110T>C
ENST00000491092.1:n.739+110T>C
NM_003058.3:c.842+110T>C	NP_003049.2:n.842+110T>C
NM_003058.4:c.842+110T>C MANE Select	NP_003049.2:n.842+110T>C