Canonical Allele Identifier: CA1931514561
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845986T= , CM000672.2:g.99845986T= GRCh38
NC_000010.10:g.101605743T= , CM000672.1:g.101605743T= GRCh37
NC_000010.9:g.101595733T= NCBI36
NG_011798.1:g.68281T=
NG_011798.2:g.68389T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146+204T= MANE Select ENSP00000497274.1:n.4146+204T=
ENST00000648523.1:c.34+204T=
ENST00000649459.1:n.494+204T=
ENST00000370449.8:c.4146+204T= ENSP00000359478.4:n.4146+204T=
NM_000392.4:c.4146+204T= NP_000383.1:n.4146+204T=
XM_006717630.2:c.3450+204T= XP_006717693.1:n.3450+204T=
XR_945604.1:n.4276+204T=
XR_945605.1:n.4210+204T=
NM_000392.5:c.4146+204T= MANE Select NP_000383.2:n.4146+204T=
XM_006717630.3:c.3450+204T= XP_006717693.1:n.3450+204T=
XR_945604.3:n.4330+204T=
XR_945605.3:n.4262+204T=