Canonical Allele Identifier: CA2681069808
Gene: SLC22A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249077G>A , CM000668.2:g.160249077G>A GRCh38
NC_000006.11:g.160670109G>A , CM000668.1:g.160670109G>A GRCh37
NC_000006.10:g.160590099G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366953.8:c.842+139C>T MANE Select ENSP00000355920.3:n.842+139C>T
ENST00000366952.1:c.779+139C>T ENSP00000355919.1:n.779+139C>T
ENST00000366953.7:c.842+139C>T ENSP00000355920.3:n.842+139C>T
ENST00000491092.1:n.739+139C>T
NM_003058.3:c.842+139C>T NP_003049.2:n.842+139C>T
NM_003058.4:c.842+139C>T MANE Select NP_003049.2:n.842+139C>T