Canonical Allele Identifier: CA151166225
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs997721643

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260380_160260398del , CM000668.2:g.160260380_160260398del GRCh38
NC_000006.11:g.160681412_160681430del , CM000668.1:g.160681412_160681430del GRCh37
NC_000006.10:g.160601402_160601420del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366952.1:c.-1006_-988del ENSP00000355919.1:n.-1006_-988del