Canonical Allele Identifier: CA821619331
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs1320982332

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260374C>T , CM000668.2:g.160260374C>T GRCh38
NC_000006.11:g.160681406C>T , CM000668.1:g.160681406C>T GRCh37
NC_000006.10:g.160601396C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-983G>A ENSP00000355919.1:n.-983G>A