Canonical Allele Identifier: CA2610497292

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99836376-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836376A>C , CM000672.2:g.99836376A>C	GRCh38
NC_000010.10:g.101596133A>C , CM000672.1:g.101596133A>C	GRCh37
NC_000010.9:g.101586123A>C	NCBI36
NG_011798.1:g.58671A>C
NG_011798.2:g.58779A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3614+86A>C MANE Select	ENSP00000497274.1:n.3614+86A>C
ENST00000370449.8:c.3614+86A>C	ENSP00000359478.4:n.3614+86A>C
NM_000392.4:c.3614+86A>C	NP_000383.1:n.3614+86A>C
XM_006717630.2:c.2918+86A>C	XP_006717693.1:n.2918+86A>C
XR_945604.1:n.3803+86A>C
XR_945605.1:n.3805+86A>C
NM_000392.5:c.3614+86A>C MANE Select	NP_000383.2:n.3614+86A>C
XM_006717630.3:c.2918+86A>C	XP_006717693.1:n.2918+86A>C
XR_945604.3:n.3857+86A>C
XR_945605.3:n.3857+86A>C