Canonical Allele Identifier: CA595642543

Gene: ABCC2

Linked Data

• dbSNP Id: rs1564701797
• gnomAD v2: 10-101605559-C-CG
• gnomAD v4: 10-99845802-C-CG
• MyVariant Identifiers: chr10:g.101605559_101605560insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845805dup , CM000672.2:g.99845805dup	GRCh38
NC_000010.10:g.101605562dup , CM000672.1:g.101605562dup	GRCh37
NC_000010.9:g.101595552dup	NCBI36
NG_011798.1:g.68100dup
NG_011798.2:g.68208dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4146+23dup MANE Select	ENSP00000497274.1:n.4146+23dup
ENST00000648523.1:c.34+23dup
ENST00000649459.1:n.494+23dup
ENST00000370449.8:c.4146+23dup	ENSP00000359478.4:n.4146+23dup
NM_000392.4:c.4146+23dup	NP_000383.1:n.4146+23dup
XM_006717630.2:c.3450+23dup	XP_006717693.1:n.3450+23dup
XR_945604.1:n.4276+23dup
XR_945605.1:n.4210+23dup
NM_000392.5:c.4146+23dup MANE Select	NP_000383.2:n.4146+23dup
XM_006717630.3:c.3450+23dup	XP_006717693.1:n.3450+23dup
XR_945604.3:n.4330+23dup
XR_945605.3:n.4262+23dup