Canonical Allele Identifier: CA2681072578
Gene: SLC22A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260382A>G , CM000668.2:g.160260382A>G GRCh38
NC_000006.11:g.160681414A>G , CM000668.1:g.160681414A>G GRCh37
NC_000006.10:g.160601404A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-991T>C ENSP00000355919.1:n.-991T>C