Canonical Allele Identifier: CA222928529
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs935316911

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61829657G>T , CM000673.2:g.61829657G>T GRCh38
NC_000011.9:g.61597129G>T , CM000673.1:g.61597129G>T GRCh37
NC_000011.8:g.61353705G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.207+1060G>T MANE Select ENSP00000278840.4:n.207+1060G>T
ENST00000257261.10:c.142-8121G>T ENSP00000257261.6:n.142-8121G>T
ENST00000278840.8:c.207+1060G>T ENSP00000278840.4:n.207+1060G>T
ENST00000517312.5:c.-160+1060G>T ENSP00000430225.1:n.-160+1060G>T
ENST00000518606.5:c.-160+2226G>T ENSP00000430054.1:n.-160+2226G>T
ENST00000521849.5:c.207+1060G>T ENSP00000431091.1:n.207+1060G>T
ENST00000522056.5:c.115-8121G>T ENSP00000429500.1:n.115-8121G>T
NM_001281501.1:c.142-8121G>T NP_001268430.1:n.142-8121G>T
NM_001281502.1:c.115-8121G>T NP_001268431.1:n.115-8121G>T
NM_004265.3:c.207+1060G>T NP_004256.1:n.207+1060G>T
XM_011545395.1:c.207+1060G>T XP_011543697.1:n.207+1060G>T
NM_004265.4:c.207+1060G>T MANE Select NP_004256.1:n.207+1060G>T