Canonical Allele Identifier: CA1977477219
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs2067159294
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61834981del , CM000673.2:g.61834981del GRCh38
NC_000011.9:g.61602453del , CM000673.1:g.61602453del GRCh37
NC_000011.8:g.61359029del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.208-2797del MANE Select ENSP00000278840.4:n.208-2797del
ENST00000257261.10:c.142-2797del ENSP00000257261.6:n.142-2797del
ENST00000278840.8:c.208-2797del ENSP00000278840.4:n.208-2797del
ENST00000517312.5:c.-159-2797del ENSP00000430225.1:n.-159-2797del
ENST00000518606.5:c.-159-2797del ENSP00000430054.1:n.-159-2797del
ENST00000521849.5:c.208-2797del ENSP00000431091.1:n.208-2797del
ENST00000522056.5:c.115-2797del ENSP00000429500.1:n.115-2797del
NM_001281501.1:c.142-2797del NP_001268430.1:n.142-2797del
NM_001281502.1:c.115-2797del NP_001268431.1:n.115-2797del
NM_004265.3:c.208-2797del NP_004256.1:n.208-2797del
XM_011545395.1:c.208-2797del XP_011543697.1:n.208-2797del
NM_004265.4:c.208-2797del MANE Select NP_004256.1:n.208-2797del
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