Canonical Allele Identifier: CA1676979835
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs1783361136

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260391T>C , CM000668.2:g.160260391T>C GRCh38
NC_000006.11:g.160681423T>C , CM000668.1:g.160681423T>C GRCh37
NC_000006.10:g.160601413T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-1000A>G ENSP00000355919.1:n.-1000A>G