Canonical Allele Identifier: CA1931512488

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038993721

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844696G>A , CM000672.2:g.99844696G>A	GRCh38
NC_000010.10:g.101604453G>A , CM000672.1:g.101604453G>A	GRCh37
NC_000010.9:g.101594443G>A	NCBI36
NG_011798.1:g.66991G>A
NG_011798.2:g.67099G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+231G>A MANE Select	ENSP00000497274.1:n.3987+231G>A
ENST00000649459.1:n.335+231G>A
ENST00000370449.8:c.3987+231G>A	ENSP00000359478.4:n.3987+231G>A
NM_000392.4:c.3987+231G>A	NP_000383.1:n.3987+231G>A
XM_006717630.2:c.3291+231G>A	XP_006717693.1:n.3291+231G>A
XR_945604.1:n.4176+231G>A
XR_945605.1:n.4051+231G>A
NM_000392.5:c.3987+231G>A MANE Select	NP_000383.2:n.3987+231G>A
XM_006717630.3:c.3291+231G>A	XP_006717693.1:n.3291+231G>A
XR_945604.3:n.4230+231G>A
XR_945605.3:n.4103+231G>A