Canonical Allele Identifier: CA670634318

Gene: ABCC2

Linked Data

• dbSNP Id: rs1279829910
• gnomAD v4: 10-99836071-TCTTTA-T
• MyVariant Identifiers: chr10:g.101595829_101595833del (hg19) ; chr10:g.99836072_99836076del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836076_99836080del , CM000672.2:g.99836076_99836080del	GRCh38
NC_000010.10:g.101595833_101595837del , CM000672.1:g.101595833_101595837del	GRCh37
NC_000010.9:g.101585823_101585827del	NCBI36
NG_011798.1:g.58371_58375del
NG_011798.2:g.58479_58483del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-15_3415-11del MANE Select	ENSP00000497274.1:n.3415-15_3415-11del
ENST00000370449.8:c.3415-15_3415-11del	ENSP00000359478.4:n.3415-15_3415-11del
NM_000392.4:c.3415-15_3415-11del	NP_000383.1:n.3415-15_3415-11del
XM_006717630.2:c.2719-15_2719-11del	XP_006717693.1:n.2719-15_2719-11del
XR_945604.1:n.3604-15_3604-11del
XR_945605.1:n.3606-15_3606-11del
NM_000392.5:c.3415-15_3415-11del MANE Select	NP_000383.2:n.3415-15_3415-11del
XM_006717630.3:c.2719-15_2719-11del	XP_006717693.1:n.2719-15_2719-11del
XR_945604.3:n.3658-15_3658-11del
XR_945605.3:n.3658-15_3658-11del