Canonical Allele Identifier: CA380861503
Gene: FADS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.61633131G>C (hg19) chr11:g.61865659G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61865659G>C , CM000673.2:g.61865659G>C GRCh38
NC_000011.9:g.61633131G>C , CM000673.1:g.61633131G>C GRCh37
NC_000011.8:g.61389707G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.1305G>C MANE Select ENSP00000278840.4:p.Lys435Asn
ENST00000257261.10:c.1239G>C ENSP00000257261.6:p.Lys413Asn
ENST00000278840.8:c.1305G>C ENSP00000278840.4:p.Lys435Asn
ENST00000522056.5:c.1212G>C ENSP00000429500.1:p.Lys404Asn
ENST00000523235.5:n.3385G>C
NM_001281501.1:c.1239G>C NP_001268430.1:p.Lys413Asn
NM_001281502.1:c.1212G>C NP_001268431.1:p.Lys404Asn
NM_004265.3:c.1305G>C NP_004256.1:p.Lys435Asn
NM_004265.4:c.1305G>C MANE Select NP_004256.1:p.Lys435Asn
Search 100 bp 5'
Search 100 bp 3'