Canonical Allele Identifier: CA2610497839
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845510_99845516del , CM000672.2:g.99845510_99845516del GRCh38
NC_000010.10:g.101605267_101605273del , CM000672.1:g.101605267_101605273del GRCh37
NC_000010.9:g.101595257_101595263del NCBI36
NG_011798.1:g.67805_67811del
NG_011798.2:g.67913_67919del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3988-114_3988-108del MANE Select ENSP00000497274.1:n.3988-114_3988-108del
ENST00000649459.1:n.336-114_336-108del
ENST00000370449.8:c.3988-114_3988-108del ENSP00000359478.4:n.3988-114_3988-108del
NM_000392.4:c.3988-114_3988-108del NP_000383.1:n.3988-114_3988-108del
XM_006717630.2:c.3292-114_3292-108del XP_006717693.1:n.3292-114_3292-108del
XR_945604.1:n.4177-173_4177-167del
XR_945605.1:n.4052-114_4052-108del
NM_000392.5:c.3988-114_3988-108del MANE Select NP_000383.2:n.3988-114_3988-108del
XM_006717630.3:c.3292-114_3292-108del XP_006717693.1:n.3292-114_3292-108del
XR_945604.3:n.4231-173_4231-167del
XR_945605.3:n.4104-114_4104-108del