Canonical Allele Identifier: CA1676979831
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260387G= , CM000668.2:g.160260387G= GRCh38
NC_000006.11:g.160681419G= , CM000668.1:g.160681419G= GRCh37
NC_000006.10:g.160601409G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-996C= ENSP00000355919.1:n.-996C=