Canonical Allele Identifier: CA1977474999
Gene: FADS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61829776C= , CM000673.2:g.61829776C= GRCh38
NC_000011.9:g.61597248C= , CM000673.1:g.61597248C= GRCh37
NC_000011.8:g.61353824C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.207+1179C= MANE Select ENSP00000278840.4:n.207+1179C=
ENST00000257261.10:c.142-8002C= ENSP00000257261.6:n.142-8002C=
ENST00000278840.8:c.207+1179C= ENSP00000278840.4:n.207+1179C=
ENST00000517312.5:c.-160+1179C= ENSP00000430225.1:n.-160+1179C=
ENST00000518606.5:c.-160+2345C= ENSP00000430054.1:n.-160+2345C=
ENST00000521849.5:c.207+1179C= ENSP00000431091.1:n.207+1179C=
ENST00000522056.5:c.115-8002C= ENSP00000429500.1:n.115-8002C=
NM_001281501.1:c.142-8002C= NP_001268430.1:n.142-8002C=
NM_001281502.1:c.115-8002C= NP_001268431.1:n.115-8002C=
NM_004265.3:c.207+1179C= NP_004256.1:n.207+1179C=
XM_011545395.1:c.207+1179C= XP_011543697.1:n.207+1179C=
NM_004265.4:c.207+1179C= MANE Select NP_004256.1:n.207+1179C=