Canonical Allele Identifier: CA151166252

Gene: SLC22A2

Linked Data

• dbSNP Id: rs532966927
• gnomAD v2: 6-160681419-G-A
• gnomAD v3: 6-160260387-G-A
• gnomAD v4: 6-160260387-G-A
• MyVariant Identifiers: chr6:g.160681419G>A (hg19) ; chr6:g.160260387G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160260387G>A , CM000668.2:g.160260387G>A	GRCh38
NC_000006.11:g.160681419G>A , CM000668.1:g.160681419G>A	GRCh37
NC_000006.10:g.160601409G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366952.1:c.-996C>T	ENSP00000355919.1:n.-996C>T