Canonical Allele Identifier: CA471130896

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101577139A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817382A>G , CM000672.2:g.99817382A>G	GRCh38
NC_000010.10:g.101577139A>G , CM000672.1:g.101577139A>G	GRCh37
NC_000010.9:g.101567129A>G	NCBI36
NG_011798.1:g.39677A>G
NG_011798.2:g.39785A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2169A>G MANE Select	ENSP00000497274.1:p.Thr723=
ENST00000370449.8:c.2169A>G	ENSP00000359478.4:p.Thr723=
NM_000392.4:c.2169A>G	NP_000383.1:p.Thr723=
XM_006717630.2:c.1473A>G	XP_006717693.1:p.Thr491=
XM_006717631.2:c.2169A>G	XP_006717694.1:p.Thr723=
XM_011539291.1:c.2169A>G	XP_011537593.1:p.Thr723=
XR_945604.1:n.2358A>G
XR_945605.1:n.2360A>G
NM_000392.5:c.2169A>G MANE Select	NP_000383.2:p.Thr723=
XM_006717630.3:c.1473A>G	XP_006717693.1:p.Thr491=
XM_006717631.4:c.2169A>G	XP_006717694.1:p.Thr723=
XM_011539291.3:c.2169A>G	XP_011537593.1:p.Thr723=
XM_017015675.2:c.2169A>G	XP_016871164.1:p.Thr723=
XR_945604.3:n.2412A>G
XR_945605.3:n.2412A>G