Canonical Allele Identifier: CA5644042
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs770515603

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845795del , CM000672.2:g.99845795del GRCh38
NC_000010.10:g.101605552del , CM000672.1:g.101605552del GRCh37
NC_000010.9:g.101595542del NCBI36
NG_011798.1:g.68090del
NG_011798.2:g.68198del

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146+13del MANE Select ENSP00000497274.1:n.4146+13del
ENST00000648523.1:c.34+13del
ENST00000649459.1:n.494+13del
ENST00000370449.8:c.4146+13del ENSP00000359478.4:n.4146+13del
NM_000392.4:c.4146+13del NP_000383.1:n.4146+13del
XM_006717630.2:c.3450+13del XP_006717693.1:n.3450+13del
XR_945604.1:n.4276+13del
XR_945605.1:n.4210+13del
NM_000392.5:c.4146+13del MANE Select NP_000383.2:n.4146+13del
XM_006717630.3:c.3450+13del XP_006717693.1:n.3450+13del
XR_945604.3:n.4330+13del
XR_945605.3:n.4262+13del