Canonical Allele Identifier: CA1931495800

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038811875

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835834_99835835del , CM000672.2:g.99835834_99835835del	GRCh38
NC_000010.10:g.101595591_101595592del , CM000672.1:g.101595591_101595592del	GRCh37
NC_000010.9:g.101585581_101585582del	NCBI36
NG_011798.1:g.58129_58130del
NG_011798.2:g.58237_58238del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-257_3415-256del MANE Select	ENSP00000497274.1:n.3415-257_3415-256del
ENST00000370449.8:c.3415-257_3415-256del	ENSP00000359478.4:n.3415-257_3415-256del
NM_000392.4:c.3415-257_3415-256del	NP_000383.1:n.3415-257_3415-256del
XM_006717630.2:c.2719-257_2719-256del	XP_006717693.1:n.2719-257_2719-256del
XR_945604.1:n.3604-257_3604-256del
XR_945605.1:n.3606-257_3606-256del
NM_000392.5:c.3415-257_3415-256del MANE Select	NP_000383.2:n.3415-257_3415-256del
XM_006717630.3:c.2719-257_2719-256del	XP_006717693.1:n.2719-257_2719-256del
XR_945604.3:n.3658-257_3658-256del
XR_945605.3:n.3658-257_3658-256del