Canonical Allele Identifier: CA5644048

Gene: ABCC2

Linked Data

• dbSNP Id: rs745464416
• ExAC: 10:101605561 G / A
• gnomAD v2: 10-101605561-G-A
• gnomAD v3: 10-99845804-G-A
• gnomAD v4: 10-99845804-G-A
• MyVariant Identifiers: chr10:g.101605561G>A (hg19) ; chr10:g.99845804G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845804G>A , CM000672.2:g.99845804G>A	GRCh38
NC_000010.10:g.101605561G>A , CM000672.1:g.101605561G>A	GRCh37
NC_000010.9:g.101595551G>A	NCBI36
NG_011798.1:g.68099G>A
NG_011798.2:g.68207G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+22G>A MANE Select	ENSP00000497274.1:n.4146+22G>A
ENST00000648523.1:c.34+22G>A
ENST00000649459.1:n.494+22G>A
ENST00000370449.8:c.4146+22G>A	ENSP00000359478.4:n.4146+22G>A
NM_000392.4:c.4146+22G>A	NP_000383.1:n.4146+22G>A
XM_006717630.2:c.3450+22G>A	XP_006717693.1:n.3450+22G>A
XR_945604.1:n.4276+22G>A
XR_945605.1:n.4210+22G>A
NM_000392.5:c.4146+22G>A MANE Select	NP_000383.2:n.4146+22G>A
XM_006717630.3:c.3450+22G>A	XP_006717693.1:n.3450+22G>A
XR_945604.3:n.4330+22G>A
XR_945605.3:n.4262+22G>A