Canonical Allele Identifier: CA378128145

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605460G>A (hg19) ; chr10:g.99845703G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845703G>A , CM000672.2:g.99845703G>A	GRCh38
NC_000010.10:g.101605460G>A , CM000672.1:g.101605460G>A	GRCh37
NC_000010.9:g.101595450G>A	NCBI36
NG_011798.1:g.67998G>A
NG_011798.2:g.68106G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4067G>A MANE Select	ENSP00000497274.1:p.Gly1356Asp
ENST00000649459.1:n.415G>A
ENST00000370449.8:c.4067G>A	ENSP00000359478.4:p.Gly1356Asp
NM_000392.4:c.4067G>A	NP_000383.1:p.Gly1356Asp
XM_006717630.2:c.3371G>A	XP_006717693.1:p.Gly1124Asp
XR_945604.1:n.4197G>A
XR_945605.1:n.4131G>A
NM_000392.5:c.4067G>A MANE Select	NP_000383.2:p.Gly1356Asp
XM_006717630.3:c.3371G>A	XP_006717693.1:p.Gly1124Asp
XR_945604.3:n.4251G>A
XR_945605.3:n.4183G>A