Canonical Allele Identifier: CA378124446

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101595894T>G (hg19) ; chr10:g.99836137T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836137T>G , CM000672.2:g.99836137T>G	GRCh38
NC_000010.10:g.101595894T>G , CM000672.1:g.101595894T>G	GRCh37
NC_000010.9:g.101585884T>G	NCBI36
NG_011798.1:g.58432T>G
NG_011798.2:g.58540T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3461T>G MANE Select	ENSP00000497274.1:p.Val1154Gly
ENST00000370449.8:c.3461T>G	ENSP00000359478.4:p.Val1154Gly
NM_000392.4:c.3461T>G	NP_000383.1:p.Val1154Gly
XM_006717630.2:c.2765T>G	XP_006717693.1:p.Val922Gly
XR_945604.1:n.3650T>G
XR_945605.1:n.3652T>G
NM_000392.5:c.3461T>G MANE Select	NP_000383.2:p.Val1154Gly
XM_006717630.3:c.2765T>G	XP_006717693.1:p.Val922Gly
XR_945604.3:n.3704T>G
XR_945605.3:n.3704T>G