Canonical Allele Identifier: CA821619345

Gene: SLC22A2

Linked Data

• dbSNP Id: rs1440673215
• gnomAD v3: 6-160260402-C-G
• gnomAD v4: 6-160260402-C-G
• MyVariant Identifiers: chr6:g.160681434C>G (hg19) ; chr6:g.160260402C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160260402C>G , CM000668.2:g.160260402C>G	GRCh38
NC_000006.11:g.160681434C>G , CM000668.1:g.160681434C>G	GRCh37
NC_000006.10:g.160601424C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366952.1:c.-1011G>C	ENSP00000355919.1:n.-1011G>C