Canonical Allele Identifier: CA1931511364

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038465888

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818643_99818644insATAAT , CM000672.2:g.99818643_99818644insATAAT	GRCh38
NC_000010.10:g.101578400_101578401insATAAT , CM000672.1:g.101578400_101578401insATAAT	GRCh37
NC_000010.9:g.101568390_101568391insATAAT	NCBI36
NG_011798.1:g.40938_40939insATAAT
NG_011798.2:g.41046_41047insATAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2272-147_2272-146insATAAT MANE Select	ENSP00000497274.1:n.2272-147_2272-146insATAAT
ENST00000370449.8:c.2272-147_2272-146insATAAT	ENSP00000359478.4:n.2272-147_2272-146insATAAT
NM_000392.4:c.2272-147_2272-146insATAAT	NP_000383.1:n.2272-147_2272-146insATAAT
XM_006717630.2:c.1576-147_1576-146insATAAT	XP_006717693.1:n.1576-147_1576-146insATAAT
XM_006717631.2:c.2272-147_2272-146insATAAT	XP_006717694.1:n.2272-147_2272-146insATAAT
XM_011539291.1:c.2272-147_2272-146insATAAT	XP_011537593.1:n.2272-147_2272-146insATAAT
XR_945604.1:n.2461-147_2461-146insATAAT
XR_945605.1:n.2463-147_2463-146insATAAT
NM_000392.5:c.2272-147_2272-146insATAAT MANE Select	NP_000383.2:n.2272-147_2272-146insATAAT
XM_006717630.3:c.1576-147_1576-146insATAAT	XP_006717693.1:n.1576-147_1576-146insATAAT
XM_006717631.4:c.2272-147_2272-146insATAAT	XP_006717694.1:n.2272-147_2272-146insATAAT
XM_011539291.3:c.2272-147_2272-146insATAAT	XP_011537593.1:n.2272-147_2272-146insATAAT
XM_017015675.2:c.2272-147_2272-146insATAAT	XP_016871164.1:n.2272-147_2272-146insATAAT
XR_945604.3:n.2515-147_2515-146insATAAT
XR_945605.3:n.2515-147_2515-146insATAAT