Canonical Allele Identifier: CA599523741
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs1195194576
gnomAD v2: 11-61633163-G-A
MyVariant Identifiers: chr11:g.61633163G>A (hg19) chr11:g.61865691G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61865691G>A , CM000673.2:g.61865691G>A GRCh38
NC_000011.9:g.61633163G>A , CM000673.1:g.61633163G>A GRCh37
NC_000011.8:g.61389739G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.*2G>A MANE Select ENSP00000278840.4:n.*2G>A
ENST00000257261.10:c.*2G>A ENSP00000257261.6:n.*2G>A
ENST00000278840.8:c.*2G>A ENSP00000278840.4:n.*2G>A
ENST00000522056.5:c.*2G>A ENSP00000429500.1:n.*2G>A
ENST00000523235.5:n.3417G>A
NM_001281501.1:c.*2G>A NP_001268430.1:n.*2G>A
NM_001281502.1:c.*2G>A NP_001268431.1:n.*2G>A
NM_004265.3:c.*2G>A NP_004256.1:n.*2G>A
NM_004265.4:c.*2G>A MANE Select NP_004256.1:n.*2G>A
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