Canonical Allele Identifier: CA599523858

Gene: FADS2

Linked Data

• dbSNP Id: rs964847672
• gnomAD v2: 11-61633185-G-T
• gnomAD v4: 11-61865713-G-T
• MyVariant Identifiers: chr11:g.61633185G>T (hg19) ; chr11:g.61865713G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61865713G>T , CM000673.2:g.61865713G>T	GRCh38
NC_000011.9:g.61633185G>T , CM000673.1:g.61633185G>T	GRCh37
NC_000011.8:g.61389761G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.*24G>T MANE Select	ENSP00000278840.4:n.*24G>T
ENST00000257261.10:c.*24G>T	ENSP00000257261.6:n.*24G>T
ENST00000278840.8:c.*24G>T	ENSP00000278840.4:n.*24G>T
ENST00000522056.5:c.*24G>T	ENSP00000429500.1:n.*24G>T
ENST00000523235.5:n.3439G>T
NM_001281501.1:c.*24G>T	NP_001268430.1:n.*24G>T
NM_001281502.1:c.*24G>T	NP_001268431.1:n.*24G>T
NM_004265.3:c.*24G>T	NP_004256.1:n.*24G>T
NM_004265.4:c.*24G>T MANE Select	NP_004256.1:n.*24G>T