Canonical Allele Identifier: CA2610497846

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845516-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845517del , CM000672.2:g.99845517del	GRCh38
NC_000010.10:g.101605274del , CM000672.1:g.101605274del	GRCh37
NC_000010.9:g.101595264del	NCBI36
NG_011798.1:g.67812del
NG_011798.2:g.67920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988-107del MANE Select	ENSP00000497274.1:n.3988-107del
ENST00000649459.1:n.336-107del
ENST00000370449.8:c.3988-107del	ENSP00000359478.4:n.3988-107del
NM_000392.4:c.3988-107del	NP_000383.1:n.3988-107del
XM_006717630.2:c.3292-107del	XP_006717693.1:n.3292-107del
XR_945604.1:n.4177-166del
XR_945605.1:n.4052-107del
NM_000392.5:c.3988-107del MANE Select	NP_000383.2:n.3988-107del
XM_006717630.3:c.3292-107del	XP_006717693.1:n.3292-107del
XR_945604.3:n.4231-166del
XR_945605.3:n.4104-107del