Canonical Allele Identifier: CA1676979774
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs1783358067

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260262_160260263del , CM000668.2:g.160260262_160260263del GRCh38
NC_000006.11:g.160681294_160681295del , CM000668.1:g.160681294_160681295del GRCh37
NC_000006.10:g.160601284_160601285del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-871_-870del ENSP00000355919.1:n.-871_-870del