Canonical Allele Identifier: CA471135334

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605383T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845626T>A , CM000672.2:g.99845626T>A	GRCh38
NC_000010.10:g.101605383T>A , CM000672.1:g.101605383T>A	GRCh37
NC_000010.9:g.101595373T>A	NCBI36
NG_011798.1:g.67921T>A
NG_011798.2:g.68029T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3990T>A MANE Select	ENSP00000497274.1:p.Ile1330=
ENST00000649459.1:n.338T>A
ENST00000370449.8:c.3990T>A	ENSP00000359478.4:p.Ile1330=
NM_000392.4:c.3990T>A	NP_000383.1:p.Ile1330=
XM_006717630.2:c.3294T>A	XP_006717693.1:p.Ile1098=
XR_945604.1:n.4177-57T>A
XR_945605.1:n.4054T>A
NM_000392.5:c.3990T>A MANE Select	NP_000383.2:p.Ile1330=
XM_006717630.3:c.3294T>A	XP_006717693.1:p.Ile1098=
XR_945604.3:n.4231-57T>A
XR_945605.3:n.4106T>A