Canonical Allele Identifier: CA3718066

Linked Data

dbSNP Id: rs370445372
gnomAD v2: 6-31625899-C-A
gnomAD v3: 6-31658122-C-A
gnomAD v4: 6-31658122-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658122C>A , CM000668.2:g.31658122C>A GRCh38
NC_000006.11:g.31625899C>A , CM000668.1:g.31625899C>A GRCh37
NC_000006.10:g.31733878C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.4:c.*33C>A (APOM) MANE Select ENSP00000365081.3:n.*33C>A
ENST00000375916.3:c.*33C>A (APOM) ENSP00000365081.3:n.*33C>A
ENST00000375920.8:c.*33C>A (APOM) ENSP00000365085.4:n.*33C>A
NM_001256169.1:c.*33C>A (APOM) NP_001243098.1:n.*33C>A
NM_019101.2:c.*33C>A (APOM) NP_061974.2:n.*33C>A
NR_045828.1:n.635C>A (APOM)
XM_006715150.2:c.*33C>A (APOM) XP_006715213.1:n.*33C>A
XM_011514895.1:c.-14+2199G>T (BAG6) XP_011513197.1:n.-14+2199G>T
XM_006715150.3:c.*33C>A (APOM) XP_006715213.1:n.*33C>A
XM_017011279.2:c.-14+2199G>T (BAG6) XP_016866768.1:n.-14+2199G>T
NM_019101.3:c.*33C>A (APOM) MANE Select NP_061974.2:n.*33C>A
NM_001256169.2:c.*33C>A (APOM) NP_001243098.1:n.*33C>A
NR_045828.2:n.641C>A (APOM)