Canonical Allele Identifier: CA378126646

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101604085T>G (hg19) ; chr10:g.99844328T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844328T>G , CM000672.2:g.99844328T>G	GRCh38
NC_000010.10:g.101604085T>G , CM000672.1:g.101604085T>G	GRCh37
NC_000010.9:g.101594075T>G	NCBI36
NG_011798.1:g.66623T>G
NG_011798.2:g.66731T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3850T>G MANE Select	ENSP00000497274.1:p.Trp1284Gly
ENST00000649459.1:n.198T>G
ENST00000370449.8:c.3850T>G	ENSP00000359478.4:p.Trp1284Gly
NM_000392.4:c.3850T>G	NP_000383.1:p.Trp1284Gly
XM_006717630.2:c.3154T>G	XP_006717693.1:p.Trp1052Gly
XR_945604.1:n.4039T>G
XR_945605.1:n.3914T>G
NM_000392.5:c.3850T>G MANE Select	NP_000383.2:p.Trp1284Gly
XM_006717630.3:c.3154T>G	XP_006717693.1:p.Trp1052Gly
XR_945604.3:n.4093T>G
XR_945605.3:n.3966T>G