Canonical Allele Identifier: CA3718068

Linked Data

dbSNP Id: rs749417439
gnomAD v2: 6-31625910-G-T
gnomAD v3: 6-31658133-G-T
gnomAD v4: 6-31658133-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658133G>T , CM000668.2:g.31658133G>T GRCh38
NC_000006.11:g.31625910G>T , CM000668.1:g.31625910G>T GRCh37
NC_000006.10:g.31733889G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.*44G>T (APOM) MANE Select ENSP00000365081.3:n.*44G>T
ENST00000375916.3:c.*44G>T (APOM) ENSP00000365081.3:n.*44G>T
ENST00000375920.8:c.*44G>T (APOM) ENSP00000365085.4:n.*44G>T
NM_001256169.1:c.*44G>T (APOM) NP_001243098.1:n.*44G>T
NM_019101.2:c.*44G>T (APOM) NP_061974.2:n.*44G>T
NR_045828.1:n.646G>T (APOM)
XM_006715150.2:c.*44G>T (APOM) XP_006715213.1:n.*44G>T
XM_011514895.1:c.-14+2188C>A (BAG6) XP_011513197.1:n.-14+2188C>A
XM_006715150.3:c.*44G>T (APOM) XP_006715213.1:n.*44G>T
XM_017011279.2:c.-14+2188C>A (BAG6) XP_016866768.1:n.-14+2188C>A
NM_019101.3:c.*44G>T (APOM) MANE Select NP_061974.2:n.*44G>T
NM_001256169.2:c.*44G>T (APOM) NP_001243098.1:n.*44G>T
NR_045828.2:n.652G>T (APOM)