Canonical Allele Identifier: CA151166229
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs973887992

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260385G>A , CM000668.2:g.160260385G>A GRCh38
NC_000006.11:g.160681417G>A , CM000668.1:g.160681417G>A GRCh37
NC_000006.10:g.160601407G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-994C>T ENSP00000355919.1:n.-994C>T