Canonical Allele Identifier: CA2610497710

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99844272-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844272G>A , CM000672.2:g.99844272G>A	GRCh38
NC_000010.10:g.101604029G>A , CM000672.1:g.101604029G>A	GRCh37
NC_000010.9:g.101594019G>A	NCBI36
NG_011798.1:g.66567G>A
NG_011798.2:g.66675G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-50G>A MANE Select	ENSP00000497274.1:n.3844-50G>A
ENST00000649459.1:n.192-50G>A
ENST00000370449.8:c.3844-50G>A	ENSP00000359478.4:n.3844-50G>A
NM_000392.4:c.3844-50G>A	NP_000383.1:n.3844-50G>A
XM_006717630.2:c.3148-50G>A	XP_006717693.1:n.3148-50G>A
XR_945604.1:n.4033-50G>A
XR_945605.1:n.3908-50G>A
NM_000392.5:c.3844-50G>A MANE Select	NP_000383.2:n.3844-50G>A
XM_006717630.3:c.3148-50G>A	XP_006717693.1:n.3148-50G>A
XR_945604.3:n.4087-50G>A
XR_945605.3:n.3960-50G>A