Canonical Allele Identifier: CA151166147

Gene: SLC22A2

Linked Data

• dbSNP Id: rs1055582819
• MyVariant Identifiers: chr6:g.160260290G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160260290G>C , CM000668.2:g.160260290G>C	GRCh38
NC_000006.11:g.160681322G>C , CM000668.1:g.160681322G>C	GRCh37
NC_000006.10:g.160601312G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366952.1:c.-899C>G	ENSP00000355919.1:n.-899C>G