Canonical Allele Identifier: CA222953379
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs482548
MyVariant Identifiers: chr11:g.61633182C>G (hg19) chr11:g.61865710C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61865710C>G , CM000673.2:g.61865710C>G GRCh38
NC_000011.9:g.61633182C>G , CM000673.1:g.61633182C>G GRCh37
NC_000011.8:g.61389758C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.*21C>G MANE Select ENSP00000278840.4:n.*21C>G
ENST00000257261.10:c.*21C>G ENSP00000257261.6:n.*21C>G
ENST00000278840.8:c.*21C>G ENSP00000278840.4:n.*21C>G
ENST00000522056.5:c.*21C>G ENSP00000429500.1:n.*21C>G
ENST00000523235.5:n.3436C>G
NM_001281501.1:c.*21C>G NP_001268430.1:n.*21C>G
NM_001281502.1:c.*21C>G NP_001268431.1:n.*21C>G
NM_004265.3:c.*21C>G NP_004256.1:n.*21C>G
NM_004265.4:c.*21C>G MANE Select NP_004256.1:n.*21C>G
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