Canonical Allele Identifier: CA378120678

Gene: ABCC2

Linked Data

• COSMIC: COSM4745641
• MyVariant Identifiers: chr10:g.101590132G>T (hg19) ; chr10:g.99830375G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830375G>T , CM000672.2:g.99830375G>T	GRCh38
NC_000010.10:g.101590132G>T , CM000672.1:g.101590132G>T	GRCh37
NC_000010.9:g.101580122G>T	NCBI36
NG_011798.1:g.52670G>T
NG_011798.2:g.52778G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2689G>T MANE Select	ENSP00000497274.1:p.Asp897Tyr
ENST00000370449.8:c.2689G>T	ENSP00000359478.4:p.Asp897Tyr
NM_000392.4:c.2689G>T	NP_000383.1:p.Asp897Tyr
XM_006717630.2:c.1993G>T	XP_006717693.1:p.Asp665Tyr
XM_006717631.2:c.*116G>T	XP_006717694.1:n.*116G>T
XM_011539291.1:c.2689G>T	XP_011537593.1:p.Asp897Tyr
XR_945604.1:n.2878G>T
XR_945605.1:n.2880G>T
NM_000392.5:c.2689G>T MANE Select	NP_000383.2:p.Asp897Tyr
XM_006717630.3:c.1993G>T	XP_006717693.1:p.Asp665Tyr
XM_006717631.4:c.*116G>T	XP_006717694.1:n.*116G>T
XM_011539291.3:c.2689G>T	XP_011537593.1:p.Asp897Tyr
XR_945604.3:n.2932G>T
XR_945605.3:n.2932G>T