Canonical Allele Identifier: CA151166123

Gene: SLC22A2

Linked Data

• dbSNP Id: rs982138901
• gnomAD v3: 6-160260274-C-T
• gnomAD v4: 6-160260274-C-T
• MyVariant Identifiers: chr6:g.160681306C>T (hg19) ; chr6:g.160260274C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160260274C>T , CM000668.2:g.160260274C>T	GRCh38
NC_000006.11:g.160681306C>T , CM000668.1:g.160681306C>T	GRCh37
NC_000006.10:g.160601296C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366952.1:c.-883G>A	ENSP00000355919.1:n.-883G>A