Canonical Allele Identifier: CA1977496582

Gene: FADS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61857233T= , CM000673.2:g.61857233T=	GRCh38
NC_000011.9:g.61624705T= , CM000673.1:g.61624705T=	GRCh37
NC_000011.8:g.61381281T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004265.4:c.805+162T= MANE Select	NP_004256.1:n.805+162T=
ENST00000278840.9:c.805+162T= MANE Select	ENSP00000278840.4:n.805+162T=
NM_001281501.1:c.739+162T=	NP_001268430.1:n.739+162T=
NM_001281502.1:c.712+162T=	NP_001268431.1:n.712+162T=
NM_004265.3:c.805+162T=	NP_004256.1:n.805+162T=
ENST00000257261.10:c.739+162T=	ENSP00000257261.6:n.739+162T=
ENST00000278840.8:c.805+162T=	ENSP00000278840.4:n.805+162T=
ENST00000355484.3:c.103+162T=	ENSP00000437965.1:n.103+162T=
ENST00000521571.6:c.103+162T=	ENSP00000443867.1:n.103+162T=
ENST00000521849.5:c.805+162T=	ENSP00000431091.1:n.805+162T=
ENST00000522056.5:c.712+162T=	ENSP00000429500.1:n.712+162T=
ENST00000523235.5:n.2885+162T=