Canonical Allele Identifier: CA2681069693
Gene: SLC22A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160247372G>T , CM000668.2:g.160247372G>T GRCh38
NC_000006.11:g.160668404G>T , CM000668.1:g.160668404G>T GRCh37
NC_000006.10:g.160588394G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366953.8:c.843-74C>A MANE Select ENSP00000355920.3:n.843-74C>A
ENST00000366952.1:c.780-74C>A ENSP00000355919.1:n.780-74C>A
ENST00000366953.7:c.843-74C>A ENSP00000355920.3:n.843-74C>A
ENST00000491092.1:n.740-74C>A
NM_003058.3:c.843-74C>A NP_003049.2:n.843-74C>A
NM_003058.4:c.843-74C>A MANE Select NP_003049.2:n.843-74C>A