Canonical Allele Identifier: CA378126708
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1590192057

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844357T>A , CM000672.2:g.99844357T>A GRCh38
NC_000010.10:g.101604114T>A , CM000672.1:g.101604114T>A GRCh37
NC_000010.9:g.101594104T>A NCBI36
NG_011798.1:g.66652T>A
NG_011798.2:g.66760T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3879T>A MANE Select ENSP00000497274.1:p.Asp1293Glu
ENST00000649459.1:n.227T>A
ENST00000370449.8:c.3879T>A ENSP00000359478.4:p.Asp1293Glu
NM_000392.4:c.3879T>A NP_000383.1:p.Asp1293Glu
XM_006717630.2:c.3183T>A XP_006717693.1:p.Asp1061Glu
XR_945604.1:n.4068T>A
XR_945605.1:n.3943T>A
NM_000392.5:c.3879T>A MANE Select NP_000383.2:p.Asp1293Glu
XM_006717630.3:c.3183T>A XP_006717693.1:p.Asp1061Glu
XR_945604.3:n.4122T>A
XR_945605.3:n.3995T>A