Canonical Allele Identifier: CA2610496267

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830397-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830399del , CM000672.2:g.99830399del	GRCh38
NC_000010.10:g.101590156del , CM000672.1:g.101590156del	GRCh37
NC_000010.9:g.101580146del	NCBI36
NG_011798.1:g.52694del
NG_011798.2:g.52802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2713del MANE Select	ENSP00000497274.1:p.Arg905GlufsTer20
ENST00000370449.8:c.2713del	ENSP00000359478.4:p.Arg905GlufsTer20
NM_000392.4:c.2713del	NP_000383.1:p.Arg905GlufsTer20
XM_006717630.2:c.2017del	XP_006717693.1:p.Arg673GlufsTer20
XM_011539291.1:c.2713del	XP_011537593.1:p.Arg905GlufsTer?
XR_945604.1:n.2902del
XR_945605.1:n.2904del
NM_000392.5:c.2713del MANE Select	NP_000383.2:p.Arg905GlufsTer20
XM_006717630.3:c.2017del	XP_006717693.1:p.Arg673GlufsTer20
XM_011539291.3:c.2713del	XP_011537593.1:p.Arg905GlufsTer?
XR_945604.3:n.2956del
XR_945605.3:n.2956del