Canonical Allele Identifier: CA938622032

Gene: FADS2

Linked Data

• dbSNP Id: rs2067160043
• gnomAD v3: 11-61834996-C-CCCTCCTCCCTGCCTGCCCCCAGGG
• gnomAD v4: 11-61834996-C-CCCTCCTCCCTGCCTGCCCCCAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61835011_61835034dup , CM000673.2:g.61835011_61835034dup	GRCh38
NC_000011.9:g.61602483_61602506dup , CM000673.1:g.61602483_61602506dup	GRCh37
NC_000011.8:g.61359059_61359082dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.208-2767_208-2744dup MANE Select	ENSP00000278840.4:n.208-2767_208-2744dup
ENST00000257261.10:c.142-2767_142-2744dup	ENSP00000257261.6:n.142-2767_142-2744dup
ENST00000278840.8:c.208-2767_208-2744dup	ENSP00000278840.4:n.208-2767_208-2744dup
ENST00000517312.5:c.-159-2767_-159-2744dup	ENSP00000430225.1:n.-159-2767_-159-2744dup
ENST00000518606.5:c.-159-2767_-159-2744dup	ENSP00000430054.1:n.-159-2767_-159-2744dup
ENST00000521849.5:c.208-2767_208-2744dup	ENSP00000431091.1:n.208-2767_208-2744dup
ENST00000522056.5:c.115-2767_115-2744dup	ENSP00000429500.1:n.115-2767_115-2744dup
NM_001281501.1:c.142-2767_142-2744dup	NP_001268430.1:n.142-2767_142-2744dup
NM_001281502.1:c.115-2767_115-2744dup	NP_001268431.1:n.115-2767_115-2744dup
NM_004265.3:c.208-2767_208-2744dup	NP_004256.1:n.208-2767_208-2744dup
XM_011545395.1:c.208-2767_208-2744dup	XP_011543697.1:n.208-2767_208-2744dup
NM_004265.4:c.208-2767_208-2744dup MANE Select	NP_004256.1:n.208-2767_208-2744dup