Canonical Allele Identifier: CA2681069911
Gene: SLC22A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249154dup , CM000668.2:g.160249154dup GRCh38
NC_000006.11:g.160670186dup , CM000668.1:g.160670186dup GRCh37
NC_000006.10:g.160590176dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+63dup MANE Select ENSP00000355920.3:n.842+63dup
ENST00000366952.1:c.779+63dup ENSP00000355919.1:n.779+63dup
ENST00000366953.7:c.842+63dup ENSP00000355920.3:n.842+63dup
ENST00000491092.1:n.739+63dup
NM_003058.3:c.842+63dup NP_003049.2:n.842+63dup
NM_003058.4:c.842+63dup MANE Select NP_003049.2:n.842+63dup