Canonical Allele Identifier: CA1977505267
Gene: FADS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61865615C= , CM000673.2:g.61865615C= GRCh38
NC_000011.9:g.61633087C= , CM000673.1:g.61633087C= GRCh37
NC_000011.8:g.61389663C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.1284-23C= MANE Select ENSP00000278840.4:n.1284-23C=
ENST00000257261.10:c.1218-23C= ENSP00000257261.6:n.1218-23C=
ENST00000278840.8:c.1284-23C= ENSP00000278840.4:n.1284-23C=
ENST00000522056.5:c.1191-23C= ENSP00000429500.1:n.1191-23C=
ENST00000523235.5:n.3364-23C=
NM_001281501.1:c.1218-23C= NP_001268430.1:n.1218-23C=
NM_001281502.1:c.1191-23C= NP_001268431.1:n.1191-23C=
NM_004265.3:c.1284-23C= NP_004256.1:n.1284-23C=
NM_004265.4:c.1284-23C= MANE Select NP_004256.1:n.1284-23C=