Canonical Allele Identifier: CA222921193

Gene: FADS3

Linked Data

• dbSNP Id: rs573513826
• MyVariant Identifiers: chr11:g.61641697G>A (hg19) ; chr11:g.61874225G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61874225G>A , CM000673.2:g.61874225G>A	GRCh38
NC_000011.9:g.61641697G>A , CM000673.1:g.61641697G>A	GRCh37
NC_000011.8:g.61398273G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278829.7:c.1287-360C>T MANE Select	ENSP00000278829.2:n.1287-360C>T
ENST00000278829.6:c.1287-360C>T	ENSP00000278829.2:n.1287-360C>T
ENST00000525094.5:c.298-360C>T
ENST00000525588.5:c.1203-360C>T	ENSP00000432206.1:n.1203-360C>T
ENST00000527379.5:c.638-360C>T
ENST00000527697.5:c.942-360C>T	ENSP00000431533.1:n.942-360C>T
ENST00000529404.5:n.2041-360C>T
ENST00000533676.5:n.4973-360C>T
NM_021727.4:c.1287-360C>T	NP_068373.1:n.1287-360C>T
XM_011545023.1:c.1314-360C>T	XP_011543325.1:n.1314-360C>T
XM_011545023.2:c.1314-360C>T	XP_011543325.1:n.1314-360C>T
XM_017017723.1:c.1452-360C>T	XP_016873212.1:n.1452-360C>T
XM_017017724.1:c.1425-360C>T	XP_016873213.1:n.1425-360C>T
XR_001747866.1:n.1950-360C>T
XR_001747868.1:n.1961-360C>T
NM_021727.5:c.1287-360C>T MANE Select	NP_068373.1:n.1287-360C>T