Canonical Allele Identifier: CA1676979788
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260283A= , CM000668.2:g.160260283A= GRCh38
NC_000006.11:g.160681315A= , CM000668.1:g.160681315A= GRCh37
NC_000006.10:g.160601305A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-892T= ENSP00000355919.1:n.-892T=