Canonical Allele Identifier: CA1676979830
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260386C= , CM000668.2:g.160260386C= GRCh38
NC_000006.11:g.160681418C= , CM000668.1:g.160681418C= GRCh37
NC_000006.10:g.160601408C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-995G= ENSP00000355919.1:n.-995G=