Canonical Allele Identifier: CA2589023982

Gene: ABCC2

Linked Data

• dbSNP Id: rs2133159610
• gnomAD v3: 10-99851390-TG-T
• gnomAD v4: 10-99851390-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851391del , CM000672.2:g.99851391del	GRCh38
NC_000010.10:g.101611148del , CM000672.1:g.101611148del	GRCh37
NC_000010.9:g.101601138del	NCBI36
NG_011798.1:g.73686del
NG_011798.2:g.73794del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4509-111del MANE Select	ENSP00000497274.1:n.4509-111del
ENST00000648523.1:c.579-111del
ENST00000370449.8:c.4509-111del	ENSP00000359478.4:n.4509-111del
NM_000392.4:c.4509-111del	NP_000383.1:n.4509-111del
XM_006717630.2:c.3813-111del	XP_006717693.1:n.3813-111del
XR_945605.1:n.4573-111del
NM_000392.5:c.4509-111del MANE Select	NP_000383.2:n.4509-111del
XM_006717630.3:c.3813-111del	XP_006717693.1:n.3813-111del
XR_945605.3:n.4625-111del