Canonical Allele Identifier: CA136880402

Identifiers and link-outs to other resources

dbSNP Id: rs114826514

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658209C>T , CM000668.2:g.31658209C>T GRCh38
NC_000006.10:g.31733965C>T NCBI36
NC_000006.11:g.31625986C>T , CM000668.1:g.31625986C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.3:c.*120C>T ENSP00000365081.3:p.=
ENST00000375920.8:c.*120C>T ENSP00000365085.4:p.=
NM_001256169.1:c.*120C>T (APOM) NP_001243098.1:p.=
NM_019101.2:c.*120C>T (APOM) NP_061974.2:p.=
NR_045828.1:n.722C>T (APOM)
XM_006715150.2:c.*120C>T (APOM) XP_006715213.1:p.=
XM_011514895.1:c.-14+2112G>A (BAG6) XP_011513197.1:p.=