Canonical Allele Identifier: CA679012406
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs988092241

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61830283G>A , CM000673.2:g.61830283G>A GRCh38
NC_000011.9:g.61597755G>A , CM000673.1:g.61597755G>A GRCh37
NC_000011.8:g.61354331G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.207+1686G>A MANE Select ENSP00000278840.4:n.207+1686G>A
ENST00000257261.10:c.142-7495G>A ENSP00000257261.6:n.142-7495G>A
ENST00000278840.8:c.207+1686G>A ENSP00000278840.4:n.207+1686G>A
ENST00000517312.5:c.-160+1686G>A ENSP00000430225.1:n.-160+1686G>A
ENST00000518606.5:c.-160+2852G>A ENSP00000430054.1:n.-160+2852G>A
ENST00000521849.5:c.207+1686G>A ENSP00000431091.1:n.207+1686G>A
ENST00000522056.5:c.115-7495G>A ENSP00000429500.1:n.115-7495G>A
NM_001281501.1:c.142-7495G>A NP_001268430.1:n.142-7495G>A
NM_001281502.1:c.115-7495G>A NP_001268431.1:n.115-7495G>A
NM_004265.3:c.207+1686G>A NP_004256.1:n.207+1686G>A
XM_011545395.1:c.207+1686G>A XP_011543697.1:n.207+1686G>A
NM_004265.4:c.207+1686G>A MANE Select NP_004256.1:n.207+1686G>A