Canonical Allele Identifier: CA670634217

Gene: ABCC2

Linked Data

• dbSNP Id: rs1160327326
• MyVariant Identifiers: chr10:g.101595644_101595646del (hg19) ; chr10:g.99835887_99835889del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835890_99835892del , CM000672.2:g.99835890_99835892del	GRCh38
NC_000010.10:g.101595647_101595649del , CM000672.1:g.101595647_101595649del	GRCh37
NC_000010.9:g.101585637_101585639del	NCBI36
NG_011798.1:g.58185_58187del
NG_011798.2:g.58293_58295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-201_3415-199del MANE Select	ENSP00000497274.1:n.3415-201_3415-199del
ENST00000370449.8:c.3415-201_3415-199del	ENSP00000359478.4:n.3415-201_3415-199del
NM_000392.4:c.3415-201_3415-199del	NP_000383.1:n.3415-201_3415-199del
XM_006717630.2:c.2719-201_2719-199del	XP_006717693.1:n.2719-201_2719-199del
XR_945604.1:n.3604-201_3604-199del
XR_945605.1:n.3606-201_3606-199del
NM_000392.5:c.3415-201_3415-199del MANE Select	NP_000383.2:n.3415-201_3415-199del
XM_006717630.3:c.2719-201_2719-199del	XP_006717693.1:n.2719-201_2719-199del
XR_945604.3:n.3658-201_3658-199del
XR_945605.3:n.3658-201_3658-199del