Canonical Allele Identifier: CA1676979820
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260361A= , CM000668.2:g.160260361A= GRCh38
NC_000006.11:g.160681393A= , CM000668.1:g.160681393A= GRCh37
NC_000006.10:g.160601383A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-970T= ENSP00000355919.1:n.-970T=