Canonical Allele Identifier: CA2574845004
Gene: FADS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61865703G>T , CM000673.2:g.61865703G>T GRCh38
NC_000011.9:g.61633175G>T , CM000673.1:g.61633175G>T GRCh37
NC_000011.8:g.61389751G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.*14G>T MANE Select ENSP00000278840.4:n.*14G>T
ENST00000257261.10:c.*14G>T ENSP00000257261.6:n.*14G>T
ENST00000278840.8:c.*14G>T ENSP00000278840.4:n.*14G>T
ENST00000522056.5:c.*14G>T ENSP00000429500.1:n.*14G>T
ENST00000523235.5:n.3429G>T
NM_001281501.1:c.*14G>T NP_001268430.1:n.*14G>T
NM_001281502.1:c.*14G>T NP_001268431.1:n.*14G>T
NM_004265.3:c.*14G>T NP_004256.1:n.*14G>T
NM_004265.4:c.*14G>T MANE Select NP_004256.1:n.*14G>T