Canonical Allele Identifier: CA1931514186
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845793_99845794delinsGA , CM000672.2:g.99845793_99845794delinsGA GRCh38
NC_000010.10:g.101605550_101605551delinsGA , CM000672.1:g.101605550_101605551delinsGA GRCh37
NC_000010.9:g.101595540_101595541delinsGA NCBI36
NG_011798.1:g.68088_68089delinsGA
NG_011798.2:g.68196_68197delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146+11_4146+12delinsGA MANE Select ENSP00000497274.1:n.4146+11_4146+12delins...
ENST00000648523.1:c.34+11_34+12delinsGA
ENST00000649459.1:n.494+11_494+12delinsGA
ENST00000370449.8:c.4146+11_4146+12delinsGA ENSP00000359478.4:n.4146+11_4146+12delins...
NM_000392.4:c.4146+11_4146+12delinsGA NP_000383.1:n.4146+11_4146+12delinsGA
XM_006717630.2:c.3450+11_3450+12delinsGA XP_006717693.1:n.3450+11_3450+12delinsGA
XR_945604.1:n.4276+11_4276+12delinsGA
XR_945605.1:n.4210+11_4210+12delinsGA
NM_000392.5:c.4146+11_4146+12delinsGA MANE Select NP_000383.2:n.4146+11_4146+12delinsGA
XM_006717630.3:c.3450+11_3450+12delinsGA XP_006717693.1:n.3450+11_3450+12delinsGA
XR_945604.3:n.4330+11_4330+12delinsGA
XR_945605.3:n.4262+11_4262+12delinsGA
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