Canonical Allele Identifier: CA938617501
Gene: FADS3 HGNC NCBI

Linked Data

dbSNP Id: rs1937782934

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61874150C>A , CM000673.2:g.61874150C>A GRCh38
NC_000011.9:g.61641622C>A , CM000673.1:g.61641622C>A GRCh37
NC_000011.8:g.61398198C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278829.7:c.1287-285G>T MANE Select ENSP00000278829.2:n.1287-285G>T
ENST00000278829.6:c.1287-285G>T ENSP00000278829.2:n.1287-285G>T
ENST00000525094.5:c.298-285G>T
ENST00000525588.5:c.1203-285G>T ENSP00000432206.1:n.1203-285G>T
ENST00000527379.5:c.638-285G>T
ENST00000527697.5:c.942-285G>T ENSP00000431533.1:n.942-285G>T
ENST00000529404.5:n.2041-285G>T
ENST00000533676.5:n.4973-285G>T
NM_021727.4:c.1287-285G>T NP_068373.1:n.1287-285G>T
XM_011545023.1:c.1314-285G>T XP_011543325.1:n.1314-285G>T
XM_011545023.2:c.1314-285G>T XP_011543325.1:n.1314-285G>T
XM_017017723.1:c.1452-285G>T XP_016873212.1:n.1452-285G>T
XM_017017724.1:c.1425-285G>T XP_016873213.1:n.1425-285G>T
XR_001747866.1:n.1950-285G>T
XR_001747868.1:n.1961-285G>T
NM_021727.5:c.1287-285G>T MANE Select NP_068373.1:n.1287-285G>T