Canonical Allele Identifier: CA2610498344

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99851363-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851363G>T , CM000672.2:g.99851363G>T	GRCh38
NC_000010.10:g.101611120G>T , CM000672.1:g.101611120G>T	GRCh37
NC_000010.9:g.101601110G>T	NCBI36
NG_011798.1:g.73658G>T
NG_011798.2:g.73766G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4509-139G>T MANE Select	ENSP00000497274.1:n.4509-139G>T
ENST00000648523.1:c.579-139G>T
ENST00000370449.8:c.4509-139G>T	ENSP00000359478.4:n.4509-139G>T
NM_000392.4:c.4509-139G>T	NP_000383.1:n.4509-139G>T
XM_006717630.2:c.3813-139G>T	XP_006717693.1:n.3813-139G>T
XR_945605.1:n.4573-139G>T
NM_000392.5:c.4509-139G>T MANE Select	NP_000383.2:n.4509-139G>T
XM_006717630.3:c.3813-139G>T	XP_006717693.1:n.3813-139G>T
XR_945605.3:n.4625-139G>T