Canonical Allele Identifier: CA13166689
Gene: ABCC2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3740065

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845936A>G , CM000672.2:g.99845936A>G GRCh38
NC_000010.10:g.101605693A>G , CM000672.1:g.101605693A>G GRCh37
NC_000010.9:g.101595683A>G NCBI36
NG_011798.1:g.68231A>G
NG_011798.2:g.68339A>G

Transcript Alleles

HGVS Amino-acid change
NM_000392.4:c.4146+154A>G VV NP_000383.1:p.=
XM_006717630.2:c.3450+154A>G XP_006717693.1:p.=
XR_945604.1:n.4276+154A>G
XR_945605.1:n.4210+154A>G
NM_000392.5:c.4146+154A>G VV NP_000383.2:p.=
XM_006717630.3:c.3450+154A>G XP_006717693.1:p.=
XR_945604.3:n.4330+154A>G
XR_945605.3:n.4262+154A>G
ENST00000370449.8:c.4146+154A>G ENSP00000359478.4:p.=