Canonical Allele Identifier: CA471135712
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101605539G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845782G>A , CM000672.2:g.99845782G>A GRCh38
NC_000010.10:g.101605539G>A , CM000672.1:g.101605539G>A GRCh37
NC_000010.9:g.101595529G>A NCBI36
NG_011798.1:g.68077G>A
NG_011798.2:g.68185G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146G>A MANE Select ENSP00000497274.1:p.Gln1382=
ENST00000648523.1:c.34G>A
ENST00000649459.1:n.494G>A
ENST00000370449.8:c.4146G>A ENSP00000359478.4:p.Gln1382=
NM_000392.4:c.4146G>A NP_000383.1:p.Gln1382=
XM_006717630.2:c.3450G>A XP_006717693.1:p.Gln1150=
XR_945604.1:n.4276G>A
XR_945605.1:n.4210G>A
NM_000392.5:c.4146G>A MANE Select NP_000383.2:p.Gln1382=
XM_006717630.3:c.3450G>A XP_006717693.1:p.Gln1150=
XR_945604.3:n.4330G>A
XR_945605.3:n.4262G>A