Canonical Allele Identifier: CA1676979784
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260275T= , CM000668.2:g.160260275T= GRCh38
NC_000006.11:g.160681307T= , CM000668.1:g.160681307T= GRCh37
NC_000006.10:g.160601297T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-884A= ENSP00000355919.1:n.-884A=