Canonical Allele Identifier: CA595453868

Gene: ABCC2

Linked Data

• dbSNP Id: rs1244855550
• gnomAD v2: 10-101611138-G-A
• gnomAD v3: 10-99851381-G-A
• gnomAD v4: 10-99851381-G-A
• MyVariant Identifiers: chr10:g.101611138G>A (hg19) ; chr10:g.99851381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851381G>A , CM000672.2:g.99851381G>A	GRCh38
NC_000010.10:g.101611138G>A , CM000672.1:g.101611138G>A	GRCh37
NC_000010.9:g.101601128G>A	NCBI36
NG_011798.1:g.73676G>A
NG_011798.2:g.73784G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4509-121G>A MANE Select	ENSP00000497274.1:n.4509-121G>A
ENST00000648523.1:c.579-121G>A
ENST00000370449.8:c.4509-121G>A	ENSP00000359478.4:n.4509-121G>A
NM_000392.4:c.4509-121G>A	NP_000383.1:n.4509-121G>A
XM_006717630.2:c.3813-121G>A	XP_006717693.1:n.3813-121G>A
XR_945605.1:n.4573-121G>A
NM_000392.5:c.4509-121G>A MANE Select	NP_000383.2:n.4509-121G>A
XM_006717630.3:c.3813-121G>A	XP_006717693.1:n.3813-121G>A
XR_945605.3:n.4625-121G>A