Canonical Allele Identifier: CA670634136

Gene: ABCC2

Linked Data

• dbSNP Id: rs1291264106
• gnomAD v3: 10-99835743-CTAA-C
• gnomAD v4: 10-99835743-CTAA-C
• MyVariant Identifiers: chr10:g.101595501_101595503del (hg19) ; chr10:g.99835744_99835746del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835745_99835747del , CM000672.2:g.99835745_99835747del	GRCh38
NC_000010.10:g.101595502_101595504del , CM000672.1:g.101595502_101595504del	GRCh37
NC_000010.9:g.101585492_101585494del	NCBI36
NG_011798.1:g.58040_58042del
NG_011798.2:g.58148_58150del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-346_3415-344del MANE Select	ENSP00000497274.1:n.3415-346_3415-344del
ENST00000370449.8:c.3415-346_3415-344del	ENSP00000359478.4:n.3415-346_3415-344del
NM_000392.4:c.3415-346_3415-344del	NP_000383.1:n.3415-346_3415-344del
XM_006717630.2:c.2719-346_2719-344del	XP_006717693.1:n.2719-346_2719-344del
XR_945604.1:n.3604-346_3604-344del
XR_945605.1:n.3606-346_3606-344del
NM_000392.5:c.3415-346_3415-344del MANE Select	NP_000383.2:n.3415-346_3415-344del
XM_006717630.3:c.2719-346_2719-344del	XP_006717693.1:n.2719-346_2719-344del
XR_945604.3:n.3658-346_3658-344del
XR_945605.3:n.3658-346_3658-344del