Canonical Allele Identifier: CA2789199237

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851394T>C , CM000672.2:g.99851394T>C	GRCh38
NC_000010.10:g.101611151T>C , CM000672.1:g.101611151T>C	GRCh37
NC_000010.9:g.101601141T>C	NCBI36
NG_011798.1:g.73689T>C
NG_011798.2:g.73797T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4509-108T>C MANE Select	ENSP00000497274.1:n.4509-108T>C
ENST00000648523.1:c.579-108T>C
ENST00000370449.8:c.4509-108T>C	ENSP00000359478.4:n.4509-108T>C
NM_000392.4:c.4509-108T>C	NP_000383.1:n.4509-108T>C
XM_006717630.2:c.3813-108T>C	XP_006717693.1:n.3813-108T>C
XR_945605.1:n.4573-108T>C
NM_000392.5:c.4509-108T>C MANE Select	NP_000383.2:n.4509-108T>C
XM_006717630.3:c.3813-108T>C	XP_006717693.1:n.3813-108T>C
XR_945605.3:n.4625-108T>C