Canonical Allele Identifier: CA2610497920

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845828-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845832del , CM000672.2:g.99845832del	GRCh38
NC_000010.10:g.101605589del , CM000672.1:g.101605589del	GRCh37
NC_000010.9:g.101595579del	NCBI36
NG_011798.1:g.68127del
NG_011798.2:g.68235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+50del MANE Select	ENSP00000497274.1:n.4146+50del
ENST00000648523.1:c.34+50del
ENST00000649459.1:n.494+50del
ENST00000370449.8:c.4146+50del	ENSP00000359478.4:n.4146+50del
NM_000392.4:c.4146+50del	NP_000383.1:n.4146+50del
XM_006717630.2:c.3450+50del	XP_006717693.1:n.3450+50del
XR_945604.1:n.4276+50del
XR_945605.1:n.4210+50del
NM_000392.5:c.4146+50del MANE Select	NP_000383.2:n.4146+50del
XM_006717630.3:c.3450+50del	XP_006717693.1:n.3450+50del
XR_945604.3:n.4330+50del
XR_945605.3:n.4262+50del