Canonical Allele Identifier: CA378128553
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845781A>T , CM000672.2:g.99845781A>T GRCh38
NC_000010.10:g.101605538A>T , CM000672.1:g.101605538A>T GRCh37
NC_000010.9:g.101595528A>T NCBI36
NG_011798.1:g.68076A>T
NG_011798.2:g.68184A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4145A>T MANE Select ENSP00000497274.1:p.Gln1382Leu
ENST00000648523.1:c.33A>T
ENST00000649459.1:n.493A>T
ENST00000370449.8:c.4145A>T ENSP00000359478.4:p.Gln1382Leu
NM_000392.4:c.4145A>T NP_000383.1:p.Gln1382Leu
XM_006717630.2:c.3449A>T XP_006717693.1:p.Gln1150Leu
XR_945604.1:n.4275A>T
XR_945605.1:n.4209A>T
NM_000392.5:c.4145A>T MANE Select NP_000383.2:p.Gln1382Leu
XM_006717630.3:c.3449A>T XP_006717693.1:p.Gln1150Leu
XR_945604.3:n.4329A>T
XR_945605.3:n.4261A>T