Canonical Allele Identifier: CA378130508

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101611261T>G (hg19) ; chr10:g.99851504T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851504T>G , CM000672.2:g.99851504T>G	GRCh38
NC_000010.10:g.101611261T>G , CM000672.1:g.101611261T>G	GRCh37
NC_000010.9:g.101601251T>G	NCBI36
NG_011798.1:g.73799T>G
NG_011798.2:g.73907T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4511T>G MANE Select	ENSP00000497274.1:p.Val1504Gly
ENST00000648523.1:c.581T>G
ENST00000370449.8:c.4511T>G	ENSP00000359478.4:p.Val1504Gly
NM_000392.4:c.4511T>G	NP_000383.1:p.Val1504Gly
XM_006717630.2:c.3815T>G	XP_006717693.1:p.Val1272Gly
XR_945605.1:n.4575T>G
NM_000392.5:c.4511T>G MANE Select	NP_000383.2:p.Val1504Gly
XM_006717630.3:c.3815T>G	XP_006717693.1:p.Val1272Gly
XR_945605.3:n.4627T>G