Canonical Allele Identifier: CA1977505302
Gene: FADS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61865656G= , CM000673.2:g.61865656G= GRCh38
NC_000011.9:g.61633128G= , CM000673.1:g.61633128G= GRCh37
NC_000011.8:g.61389704G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.1302G= MANE Select ENSP00000278840.4:p.Gly434=
ENST00000257261.10:c.1236G= ENSP00000257261.6:p.Gly412=
ENST00000278840.8:c.1302G= ENSP00000278840.4:p.Gly434=
ENST00000522056.5:c.1209G= ENSP00000429500.1:p.Gly403=
ENST00000523235.5:n.3382G=
NM_001281501.1:c.1236G= NP_001268430.1:p.Gly412=
NM_001281502.1:c.1209G= NP_001268431.1:p.Gly403=
NM_004265.3:c.1302G= NP_004256.1:p.Gly434=
NM_004265.4:c.1302G= MANE Select NP_004256.1:p.Gly434=