Canonical Allele Identifier: CA1977505361
Gene: FADS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61865711G= , CM000673.2:g.61865711G= GRCh38
NC_000011.9:g.61633183G= , CM000673.1:g.61633183G= GRCh37
NC_000011.8:g.61389759G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.*22G= MANE Select ENSP00000278840.4:n.*22G=
ENST00000257261.10:c.*22G= ENSP00000257261.6:n.*22G=
ENST00000278840.8:c.*22G= ENSP00000278840.4:n.*22G=
ENST00000522056.5:c.*22G= ENSP00000429500.1:n.*22G=
ENST00000523235.5:n.3437G=
NM_001281501.1:c.*22G= NP_001268430.1:n.*22G=
NM_001281502.1:c.*22G= NP_001268431.1:n.*22G=
NM_004265.3:c.*22G= NP_004256.1:n.*22G=
NM_004265.4:c.*22G= MANE Select NP_004256.1:n.*22G=
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