Canonical Allele Identifier: CA1931513914

Gene: ABCC2

Linked Data

• dbSNP Id: rs2039005942

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845683_99845700del , CM000672.2:g.99845683_99845700del	GRCh38
NC_000010.10:g.101605440_101605457del , CM000672.1:g.101605440_101605457del	GRCh37
NC_000010.9:g.101595430_101595447del	NCBI36
NG_011798.1:g.67978_67995del
NG_011798.2:g.68086_68103del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4047_4064del MANE Select	ENSP00000497274.1:p.Arg1349_Gly1355delins...
ENST00000649459.1:n.395_412del
ENST00000370449.8:c.4047_4064del	ENSP00000359478.4:p.Arg1349_Gly1355delins...
NM_000392.4:c.4047_4064del	NP_000383.1:p.Arg1349_Gly1355delinsSer
XM_006717630.2:c.3351_3368del	XP_006717693.1:p.Arg1117_Gly1123delinsSer...
XR_945604.1:n.4177_4194del
XR_945605.1:n.4111_4128del
NM_000392.5:c.4047_4064del MANE Select	NP_000383.2:p.Arg1349_Gly1355delinsSer
XM_006717630.3:c.3351_3368del	XP_006717693.1:p.Arg1117_Gly1123delinsSer...
XR_945604.3:n.4231_4248del
XR_945605.3:n.4163_4180del