Canonical Allele Identifier: CA938613338

Gene: FADS2

Linked Data

• dbSNP Id: rs2067463170
• gnomAD v3: 11-61865751-A-G
• gnomAD v4: 11-61865751-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61865751A>G , CM000673.2:g.61865751A>G	GRCh38
NC_000011.9:g.61633223A>G , CM000673.1:g.61633223A>G	GRCh37
NC_000011.8:g.61389799A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.*62A>G MANE Select	ENSP00000278840.4:n.*62A>G
ENST00000257261.10:c.*62A>G	ENSP00000257261.6:n.*62A>G
ENST00000278840.8:c.*62A>G	ENSP00000278840.4:n.*62A>G
ENST00000522056.5:c.*62A>G	ENSP00000429500.1:n.*62A>G
ENST00000523235.5:n.3477A>G
NM_001281501.1:c.*62A>G	NP_001268430.1:n.*62A>G
NM_001281502.1:c.*62A>G	NP_001268431.1:n.*62A>G
NM_004265.3:c.*62A>G	NP_004256.1:n.*62A>G
NM_004265.4:c.*62A>G MANE Select	NP_004256.1:n.*62A>G