Canonical Allele Identifier: CA670641347

Gene: ABCC2

Linked Data

• dbSNP Id: rs1383641485
• MyVariant Identifiers: chr10:g.101605305_101605306del (hg19) ; chr10:g.99845548_99845549del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845550_99845551del , CM000672.2:g.99845550_99845551del	GRCh38
NC_000010.10:g.101605307_101605308del , CM000672.1:g.101605307_101605308del	GRCh37
NC_000010.9:g.101595297_101595298del	NCBI36
NG_011798.1:g.67845_67846del
NG_011798.2:g.67953_67954del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988-74_3988-73del MANE Select	ENSP00000497274.1:n.3988-74_3988-73del
ENST00000649459.1:n.336-74_336-73del
ENST00000370449.8:c.3988-74_3988-73del	ENSP00000359478.4:n.3988-74_3988-73del
NM_000392.4:c.3988-74_3988-73del	NP_000383.1:n.3988-74_3988-73del
XM_006717630.2:c.3292-74_3292-73del	XP_006717693.1:n.3292-74_3292-73del
XR_945604.1:n.4177-133_4177-132del
XR_945605.1:n.4052-74_4052-73del
NM_000392.5:c.3988-74_3988-73del MANE Select	NP_000383.2:n.3988-74_3988-73del
XM_006717630.3:c.3292-74_3292-73del	XP_006717693.1:n.3292-74_3292-73del
XR_945604.3:n.4231-133_4231-132del
XR_945605.3:n.4104-74_4104-73del