Canonical Allele Identifier: CA1931495730

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038810361

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835761_99835762del , CM000672.2:g.99835761_99835762del	GRCh38
NC_000010.10:g.101595518_101595519del , CM000672.1:g.101595518_101595519del	GRCh37
NC_000010.9:g.101585508_101585509del	NCBI36
NG_011798.1:g.58056_58057del
NG_011798.2:g.58164_58165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-330_3415-329del MANE Select	ENSP00000497274.1:n.3415-330_3415-329del
ENST00000370449.8:c.3415-330_3415-329del	ENSP00000359478.4:n.3415-330_3415-329del
NM_000392.4:c.3415-330_3415-329del	NP_000383.1:n.3415-330_3415-329del
XM_006717630.2:c.2719-330_2719-329del	XP_006717693.1:n.2719-330_2719-329del
XR_945604.1:n.3604-330_3604-329del
XR_945605.1:n.3606-330_3606-329del
NM_000392.5:c.3415-330_3415-329del MANE Select	NP_000383.2:n.3415-330_3415-329del
XM_006717630.3:c.2719-330_2719-329del	XP_006717693.1:n.2719-330_2719-329del
XR_945604.3:n.3658-330_3658-329del
XR_945605.3:n.3658-330_3658-329del