Canonical Allele Identifier: CA471133341

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101604093T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844336T>G , CM000672.2:g.99844336T>G	GRCh38
NC_000010.10:g.101604093T>G , CM000672.1:g.101604093T>G	GRCh37
NC_000010.9:g.101594083T>G	NCBI36
NG_011798.1:g.66631T>G
NG_011798.2:g.66739T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3858T>G MANE Select	ENSP00000497274.1:p.Thr1286=
ENST00000649459.1:n.206T>G
ENST00000370449.8:c.3858T>G	ENSP00000359478.4:p.Thr1286=
NM_000392.4:c.3858T>G	NP_000383.1:p.Thr1286=
XM_006717630.2:c.3162T>G	XP_006717693.1:p.Thr1054=
XR_945604.1:n.4047T>G
XR_945605.1:n.3922T>G
NM_000392.5:c.3858T>G MANE Select	NP_000383.2:p.Thr1286=
XM_006717630.3:c.3162T>G	XP_006717693.1:p.Thr1054=
XR_945604.3:n.4101T>G
XR_945605.3:n.3974T>G