Canonical Allele Identifier: CA378128029
Gene: ABCC2 HGNC NCBI

Linked Data

COSMIC: COSM913830

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845681A>G , CM000672.2:g.99845681A>G GRCh38
NC_000010.10:g.101605438A>G , CM000672.1:g.101605438A>G GRCh37
NC_000010.9:g.101595428A>G NCBI36
NG_011798.1:g.67976A>G
NG_011798.2:g.68084A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4045A>G MANE Select ENSP00000497274.1:p.Arg1349Gly
ENST00000649459.1:n.393A>G
ENST00000370449.8:c.4045A>G ENSP00000359478.4:p.Arg1349Gly
NM_000392.4:c.4045A>G NP_000383.1:p.Arg1349Gly
XM_006717630.2:c.3349A>G XP_006717693.1:p.Arg1117Gly
XR_945604.1:n.4177-2A>G
XR_945605.1:n.4109A>G
NM_000392.5:c.4045A>G MANE Select NP_000383.2:p.Arg1349Gly
XM_006717630.3:c.3349A>G XP_006717693.1:p.Arg1117Gly
XR_945604.3:n.4231-2A>G
XR_945605.3:n.4161A>G