Canonical Allele Identifier: CA1676979783
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260274C= , CM000668.2:g.160260274C= GRCh38
NC_000006.11:g.160681306C= , CM000668.1:g.160681306C= GRCh37
NC_000006.10:g.160601296C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-883G= ENSP00000355919.1:n.-883G=