Canonical Allele Identifier: CA1931496190

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038818718
• gnomAD v4: 10-99836147-C-CAGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836147_99836148insAGGT , CM000672.2:g.99836147_99836148insAGGT	GRCh38
NC_000010.10:g.101595904_101595905insAGGT , CM000672.1:g.101595904_101595905insAGGT	GRCh37
NC_000010.9:g.101585894_101585895insAGGT	NCBI36
NG_011798.1:g.58442_58443insAGGT
NG_011798.2:g.58550_58551insAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3471_3472insAGGT MANE Select	ENSP00000497274.1:p.Pro1158ArgfsTer21
ENST00000370449.8:c.3471_3472insAGGT	ENSP00000359478.4:p.Pro1158ArgfsTer21
NM_000392.4:c.3471_3472insAGGT	NP_000383.1:p.Pro1158ArgfsTer21
XM_006717630.2:c.2775_2776insAGGT	XP_006717693.1:p.Pro926ArgfsTer21
XR_945604.1:n.3660_3661insAGGT
XR_945605.1:n.3662_3663insAGGT
NM_000392.5:c.3471_3472insAGGT MANE Select	NP_000383.2:p.Pro1158ArgfsTer21
XM_006717630.3:c.2775_2776insAGGT	XP_006717693.1:p.Pro926ArgfsTer21
XR_945604.3:n.3714_3715insAGGT
XR_945605.3:n.3714_3715insAGGT