Canonical Allele Identifier: CA2681072567
Gene: SLC22A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260365G>T , CM000668.2:g.160260365G>T GRCh38
NC_000006.11:g.160681397G>T , CM000668.1:g.160681397G>T GRCh37
NC_000006.10:g.160601387G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-974C>A ENSP00000355919.1:n.-974C>A