Canonical Allele Identifier: CA378128543

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605535C>G (hg19) ; chr10:g.99845778C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845778C>G , CM000672.2:g.99845778C>G	GRCh38
NC_000010.10:g.101605535C>G , CM000672.1:g.101605535C>G	GRCh37
NC_000010.9:g.101595525C>G	NCBI36
NG_011798.1:g.68073C>G
NG_011798.2:g.68181C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4142C>G MANE Select	ENSP00000497274.1:p.Pro1381Arg
ENST00000648523.1:c.30C>G
ENST00000649459.1:n.490C>G
ENST00000370449.8:c.4142C>G	ENSP00000359478.4:p.Pro1381Arg
NM_000392.4:c.4142C>G	NP_000383.1:p.Pro1381Arg
XM_006717630.2:c.3446C>G	XP_006717693.1:p.Pro1149Arg
XR_945604.1:n.4272C>G
XR_945605.1:n.4206C>G
NM_000392.5:c.4142C>G MANE Select	NP_000383.2:p.Pro1381Arg
XM_006717630.3:c.3446C>G	XP_006717693.1:p.Pro1149Arg
XR_945604.3:n.4326C>G
XR_945605.3:n.4258C>G