Canonical Allele Identifier: CA670634224

Gene: ABCC2

Linked Data

• dbSNP Id: rs1380957225
• MyVariant Identifiers: chr10:g.101595654_101595655del (hg19) ; chr10:g.99835897_99835898del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835897_99835898del , CM000672.2:g.99835897_99835898del	GRCh38
NC_000010.10:g.101595654_101595655del , CM000672.1:g.101595654_101595655del	GRCh37
NC_000010.9:g.101585644_101585645del	NCBI36
NG_011798.1:g.58192_58193del
NG_011798.2:g.58300_58301del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-194_3415-193del MANE Select	ENSP00000497274.1:n.3415-194_3415-193del
ENST00000370449.8:c.3415-194_3415-193del	ENSP00000359478.4:n.3415-194_3415-193del
NM_000392.4:c.3415-194_3415-193del	NP_000383.1:n.3415-194_3415-193del
XM_006717630.2:c.2719-194_2719-193del	XP_006717693.1:n.2719-194_2719-193del
XR_945604.1:n.3604-194_3604-193del
XR_945605.1:n.3606-194_3606-193del
NM_000392.5:c.3415-194_3415-193del MANE Select	NP_000383.2:n.3415-194_3415-193del
XM_006717630.3:c.2719-194_2719-193del	XP_006717693.1:n.2719-194_2719-193del
XR_945604.3:n.3658-194_3658-193del
XR_945605.3:n.3658-194_3658-193del