Canonical Allele Identifier: CA378128554
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146G>C MANE Select ENSP00000497274.1:p.Gln1382His
ENST00000648523.1:c.34G>C
ENST00000649459.1:n.494G>C
ENST00000370449.8:c.4146G>C ENSP00000359478.4:p.Gln1382His
NM_000392.4:c.4146G>C NP_000383.1:p.Gln1382His
XM_006717630.2:c.3450G>C XP_006717693.1:p.Gln1150His
XR_945604.1:n.4276G>C
XR_945605.1:n.4210G>C
NM_000392.5:c.4146G>C MANE Select NP_000383.2:p.Gln1382His
XM_006717630.3:c.3450G>C XP_006717693.1:p.Gln1150His
XR_945604.3:n.4330G>C
XR_945605.3:n.4262G>C