Canonical Allele Identifier: CA2681072571
Gene: SLC22A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260371C>A , CM000668.2:g.160260371C>A GRCh38
NC_000006.11:g.160681403C>A , CM000668.1:g.160681403C>A GRCh37
NC_000006.10:g.160601393C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-980G>T ENSP00000355919.1:n.-980G>T