Canonical Allele Identifier: CA378126644
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1265009798

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3850T>A MANE Select ENSP00000497274.1:p.Trp1284Arg
ENST00000649459.1:n.198T>A
ENST00000370449.8:c.3850T>A ENSP00000359478.4:p.Trp1284Arg
NM_000392.4:c.3850T>A NP_000383.1:p.Trp1284Arg
XM_006717630.2:c.3154T>A XP_006717693.1:p.Trp1052Arg
XR_945604.1:n.4039T>A
XR_945605.1:n.3914T>A
NM_000392.5:c.3850T>A MANE Select NP_000383.2:p.Trp1284Arg
XM_006717630.3:c.3154T>A XP_006717693.1:p.Trp1052Arg
XR_945604.3:n.4093T>A
XR_945605.3:n.3966T>A