Canonical Allele Identifier: CA670641733

Gene: ABCC2

Linked Data

• dbSNP Id: rs1437613300
• MyVariant Identifiers: chr10:g.101605596A>C (hg19) ; chr10:g.99845839A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845839A>C , CM000672.2:g.99845839A>C	GRCh38
NC_000010.10:g.101605596A>C , CM000672.1:g.101605596A>C	GRCh37
NC_000010.9:g.101595586A>C	NCBI36
NG_011798.1:g.68134A>C
NG_011798.2:g.68242A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4146+57A>C MANE Select	ENSP00000497274.1:n.4146+57A>C
ENST00000648523.1:c.34+57A>C
ENST00000649459.1:n.494+57A>C
ENST00000370449.8:c.4146+57A>C	ENSP00000359478.4:n.4146+57A>C
NM_000392.4:c.4146+57A>C	NP_000383.1:n.4146+57A>C
XM_006717630.2:c.3450+57A>C	XP_006717693.1:n.3450+57A>C
XR_945604.1:n.4276+57A>C
XR_945605.1:n.4210+57A>C
NM_000392.5:c.4146+57A>C MANE Select	NP_000383.2:n.4146+57A>C
XM_006717630.3:c.3450+57A>C	XP_006717693.1:n.3450+57A>C
XR_945604.3:n.4330+57A>C
XR_945605.3:n.4262+57A>C