Canonical Allele Identifier: CA1676974845

Gene: SLC22A2

Linked Data

• dbSNP Id: rs1783142791
• gnomAD v4: 6-160249202-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160249202C>G , CM000668.2:g.160249202C>G	GRCh38
NC_000006.11:g.160670234C>G , CM000668.1:g.160670234C>G	GRCh37
NC_000006.10:g.160590224C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366953.8:c.842+14G>C MANE Select	ENSP00000355920.3:n.842+14G>C
ENST00000366952.1:c.779+14G>C	ENSP00000355919.1:n.779+14G>C
ENST00000366953.7:c.842+14G>C	ENSP00000355920.3:n.842+14G>C
ENST00000491092.1:n.739+14G>C
NM_003058.3:c.842+14G>C	NP_003049.2:n.842+14G>C
NM_003058.4:c.842+14G>C MANE Select	NP_003049.2:n.842+14G>C