Canonical Allele Identifier: CA136880278

Identifiers and link-outs to other resources

dbSNP Id: rs116715239

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31656393G>C , CM000668.2:g.31656393G>C GRCh38
NC_000006.10:g.31732149G>C NCBI36
NC_000006.11:g.31624170G>C , CM000668.1:g.31624170G>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.3:c.115-79G>C ENSP00000365081.3:p.=
ENST00000375918.6:c.-102-79G>C ENSP00000365083.2:p.=
ENST00000375920.8:c.-102-79G>C ENSP00000365085.4:p.=
NM_001256169.1:c.-102-79G>C (APOM) VV NP_001243098.1:p.=
NM_019101.2:c.115-79G>C (APOM) VV NP_061974.2:p.=
NR_045828.1:n.143-79G>C (APOM)
XM_006715150.2:c.12-79G>C (APOM) XP_006715213.1:p.=
XM_011514895.1:c.-14+3928C>G (BAG6) XP_011513197.1:p.=