Canonical Allele Identifier: CA1096530107
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs1783360838

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260383T>C , CM000668.2:g.160260383T>C GRCh38
NC_000006.11:g.160681415T>C , CM000668.1:g.160681415T>C GRCh37
NC_000006.10:g.160601405T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-992A>G ENSP00000355919.1:n.-992A>G