Canonical Allele Identifier: CA378126702

Gene: ABCC2

Linked Data

• COSMIC: COSM4988516
• MyVariant Identifiers: chr10:g.101604112G>A (hg19) ; chr10:g.99844355G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844355G>A , CM000672.2:g.99844355G>A	GRCh38
NC_000010.10:g.101604112G>A , CM000672.1:g.101604112G>A	GRCh37
NC_000010.9:g.101594102G>A	NCBI36
NG_011798.1:g.66650G>A
NG_011798.2:g.66758G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3877G>A MANE Select	ENSP00000497274.1:p.Asp1293Asn
ENST00000649459.1:n.225G>A
ENST00000370449.8:c.3877G>A	ENSP00000359478.4:p.Asp1293Asn
NM_000392.4:c.3877G>A	NP_000383.1:p.Asp1293Asn
XM_006717630.2:c.3181G>A	XP_006717693.1:p.Asp1061Asn
XR_945604.1:n.4066G>A
XR_945605.1:n.3941G>A
NM_000392.5:c.3877G>A MANE Select	NP_000383.2:p.Asp1293Asn
XM_006717630.3:c.3181G>A	XP_006717693.1:p.Asp1061Asn
XR_945604.3:n.4120G>A
XR_945605.3:n.3993G>A