Canonical Allele Identifier: CA151166119
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs151196271

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260268G>A , CM000668.2:g.160260268G>A GRCh38
NC_000006.11:g.160681300G>A , CM000668.1:g.160681300G>A GRCh37
NC_000006.10:g.160601290G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-877C>T ENSP00000355919.1:n.-877C>T