Canonical Allele Identifier: CA378127745
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.99845614del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845614del , CM000672.2:g.99845614del GRCh38
NC_000010.10:g.101605371del , CM000672.1:g.101605371del GRCh37
NC_000010.9:g.101595361del NCBI36
NG_011798.1:g.67909del
NG_011798.2:g.68017del

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3988-10del MANE Select ENSP00000497274.1:n.3988-10del
ENST00000649459.1:n.336-10del
ENST00000370449.8:c.3988-10del ENSP00000359478.4:n.3988-10del
NM_000392.4:c.3988-10del NP_000383.1:n.3988-10del
XM_006717630.2:c.3292-10del XP_006717693.1:n.3292-10del
XR_945604.1:n.4177-69del
XR_945605.1:n.4052-10del
NM_000392.5:c.3988-10del MANE Select NP_000383.2:n.3988-10del
XM_006717630.3:c.3292-10del XP_006717693.1:n.3292-10del
XR_945604.3:n.4231-69del
XR_945605.3:n.4104-10del