Canonical Allele Identifier: CA821619281

Gene: SLC22A2

Linked Data

• dbSNP Id: rs1299957700
• gnomAD v4: 6-160260275-T-C
• MyVariant Identifiers: chr6:g.160681307T>C (hg19) ; chr6:g.160260275T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160260275T>C , CM000668.2:g.160260275T>C	GRCh38
NC_000006.11:g.160681307T>C , CM000668.1:g.160681307T>C	GRCh37
NC_000006.10:g.160601297T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366952.1:c.-884A>G	ENSP00000355919.1:n.-884A>G