Canonical Allele Identifier: CA2610497860

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845541-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845541C>A , CM000672.2:g.99845541C>A	GRCh38
NC_000010.10:g.101605298C>A , CM000672.1:g.101605298C>A	GRCh37
NC_000010.9:g.101595288C>A	NCBI36
NG_011798.1:g.67836C>A
NG_011798.2:g.67944C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988-83C>A MANE Select	ENSP00000497274.1:n.3988-83C>A
ENST00000649459.1:n.336-83C>A
ENST00000370449.8:c.3988-83C>A	ENSP00000359478.4:n.3988-83C>A
NM_000392.4:c.3988-83C>A	NP_000383.1:n.3988-83C>A
XM_006717630.2:c.3292-83C>A	XP_006717693.1:n.3292-83C>A
XR_945604.1:n.4177-142C>A
XR_945605.1:n.4052-83C>A
NM_000392.5:c.3988-83C>A MANE Select	NP_000383.2:n.3988-83C>A
XM_006717630.3:c.3292-83C>A	XP_006717693.1:n.3292-83C>A
XR_945604.3:n.4231-142C>A
XR_945605.3:n.4104-83C>A