Canonical Allele Identifier: CA378128084
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845692G>T , CM000672.2:g.99845692G>T GRCh38
NC_000010.10:g.101605449G>T , CM000672.1:g.101605449G>T GRCh37
NC_000010.9:g.101595439G>T NCBI36
NG_011798.1:g.67987G>T
NG_011798.2:g.68095G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4056G>T MANE Select ENSP00000497274.1:p.Glu1352Asp
ENST00000649459.1:n.404G>T
ENST00000370449.8:c.4056G>T ENSP00000359478.4:p.Glu1352Asp
NM_000392.4:c.4056G>T NP_000383.1:p.Glu1352Asp
XM_006717630.2:c.3360G>T XP_006717693.1:p.Glu1120Asp
XR_945604.1:n.4186G>T
XR_945605.1:n.4120G>T
NM_000392.5:c.4056G>T MANE Select NP_000383.2:p.Glu1352Asp
XM_006717630.3:c.3360G>T XP_006717693.1:p.Glu1120Asp
XR_945604.3:n.4240G>T
XR_945605.3:n.4172G>T