Canonical Allele Identifier: CA1977511521

Gene: FADS3

Linked Data

• dbSNP Id: rs1937778444

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61874054T>G , CM000673.2:g.61874054T>G	GRCh38
NC_000011.9:g.61641526T>G , CM000673.1:g.61641526T>G	GRCh37
NC_000011.8:g.61398102T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000278829.7:c.1287-189A>C MANE Select	ENSP00000278829.2:n.1287-189A>C
ENST00000278829.6:c.1287-189A>C	ENSP00000278829.2:n.1287-189A>C
ENST00000525094.5:c.298-189A>C
ENST00000525588.5:c.1203-189A>C	ENSP00000432206.1:n.1203-189A>C
ENST00000527379.5:c.638-189A>C
ENST00000527697.5:c.942-189A>C	ENSP00000431533.1:n.942-189A>C
ENST00000529404.5:n.2041-189A>C
ENST00000533676.5:n.4973-189A>C
NM_021727.4:c.1287-189A>C	NP_068373.1:n.1287-189A>C
XM_011545023.1:c.1314-189A>C	XP_011543325.1:n.1314-189A>C
XM_011545023.2:c.1314-189A>C	XP_011543325.1:n.1314-189A>C
XM_017017723.1:c.1452-189A>C	XP_016873212.1:n.1452-189A>C
XM_017017724.1:c.1425-189A>C	XP_016873213.1:n.1425-189A>C
XR_001747866.1:n.1950-189A>C
XR_001747868.1:n.1961-189A>C
NM_021727.5:c.1287-189A>C MANE Select	NP_068373.1:n.1287-189A>C