Canonical Allele Identifier: CA13418983
Gene: FADS3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1000778

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61887833A>G , CM000673.2:g.61887833A>G GRCh38
NC_000011.9:g.61655305A>G , CM000673.1:g.61655305A>G GRCh37
NC_000011.8:g.61411881A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_021727.4:c.213+3336T>C VV NP_068373.1:p.=
XM_011545023.1:c.213+3336T>C XP_011543325.1:p.=
XM_011545023.2:c.213+3336T>C
XM_017017723.1:c.351+4026T>C XP_016873212.1:p.=
XM_017017724.1:c.351+4026T>C XP_016873213.1:p.=
XR_001747866.1:n.366+4026T>C
XR_001747867.1:n.366+4026T>C
XR_001747868.1:n.377+3336T>C
XR_001747869.1:n.377+3336T>C
NM_021727.5:c.213+3336T>C VV MANE Preferred
ENST00000278829.6:c.213+3336T>C ENSP00000278829.2:p.=
ENST00000414624.6:n.286+3336T>C
ENST00000525588.5:n.213+3336T>C ENSP00000432206.1:p.=
ENST00000527697.5:c.-160+4026T>C ENSP00000431533.1:p.=