Canonical Allele Identifier: CA2581598456
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260282T>G , CM000668.2:g.160260282T>G GRCh38
NC_000006.11:g.160681314T>G , CM000668.1:g.160681314T>G GRCh37
NC_000006.10:g.160601304T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-891A>C ENSP00000355919.1:n.-891A>C