Canonical Allele Identifier: CA378120998

Gene: ABCC2

Linked Data

• dbSNP Id: rs112758556
• gnomAD v3: 10-99830429-C-A
• gnomAD v4: 10-99830429-C-A
• MyVariant Identifiers: chr10:g.101590186C>A (hg19) ; chr10:g.99830429C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830429C>A , CM000672.2:g.99830429C>A	GRCh38
NC_000010.10:g.101590186C>A , CM000672.1:g.101590186C>A	GRCh37
NC_000010.9:g.101580176C>A	NCBI36
NG_011798.1:g.52724C>A
NG_011798.2:g.52832C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2743C>A MANE Select	ENSP00000497274.1:p.Arg915Ser
ENST00000370449.8:c.2743C>A	ENSP00000359478.4:p.Arg915Ser
NM_000392.4:c.2743C>A	NP_000383.1:p.Arg915Ser
XM_006717630.2:c.2047C>A	XP_006717693.1:p.Arg683Ser
XM_011539291.1:c.2743C>A	XP_011537593.1:p.Arg915Ser
XR_945604.1:n.2932C>A
XR_945605.1:n.2934C>A
NM_000392.5:c.2743C>A MANE Select	NP_000383.2:p.Arg915Ser
XM_006717630.3:c.2047C>A	XP_006717693.1:p.Arg683Ser
XM_011539291.3:c.2743C>A	XP_011537593.1:p.Arg915Ser
XR_945604.3:n.2986C>A
XR_945605.3:n.2986C>A