Canonical Allele Identifier: CA5643435

Gene: ABCC2

Linked Data

• dbSNP Id: rs774051725
• ExAC: 10:101578512 GAGT / G
• gnomAD v2: 10-101578512-GAGT-G
• gnomAD v3: 10-99818755-GAGT-G
• gnomAD v4: 10-99818755-GAGT-G
• MyVariant Identifiers: chr10:g.101578513_101578515del (hg19) ; chr10:g.99818756_99818758del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818759_99818761del , CM000672.2:g.99818759_99818761del	GRCh38
NC_000010.10:g.101578516_101578518del , CM000672.1:g.101578516_101578518del	GRCh37
NC_000010.9:g.101568506_101568508del	NCBI36
NG_011798.1:g.41054_41056del
NG_011798.2:g.41162_41164del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2272-31_2272-29del MANE Select	ENSP00000497274.1:n.2272-31_2272-29del
ENST00000370449.8:c.2272-31_2272-29del	ENSP00000359478.4:n.2272-31_2272-29del
NM_000392.4:c.2272-31_2272-29del	NP_000383.1:n.2272-31_2272-29del
XM_006717630.2:c.1576-31_1576-29del	XP_006717693.1:n.1576-31_1576-29del
XM_006717631.2:c.2272-31_2272-29del	XP_006717694.1:n.2272-31_2272-29del
XM_011539291.1:c.2272-31_2272-29del	XP_011537593.1:n.2272-31_2272-29del
XR_945604.1:n.2461-31_2461-29del
XR_945605.1:n.2463-31_2463-29del
NM_000392.5:c.2272-31_2272-29del MANE Select	NP_000383.2:n.2272-31_2272-29del
XM_006717630.3:c.1576-31_1576-29del	XP_006717693.1:n.1576-31_1576-29del
XM_006717631.4:c.2272-31_2272-29del	XP_006717694.1:n.2272-31_2272-29del
XM_011539291.3:c.2272-31_2272-29del	XP_011537593.1:n.2272-31_2272-29del
XM_017015675.2:c.2272-31_2272-29del	XP_016871164.1:n.2272-31_2272-29del
XR_945604.3:n.2515-31_2515-29del
XR_945605.3:n.2515-31_2515-29del