Canonical Allele Identifier: CA222931727

Gene: FADS3

Linked Data

• dbSNP Id: rs183888374
• MyVariant Identifiers: chr11:g.61655321A>G (hg19) ; chr11:g.61887849A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61887849A>G , CM000673.2:g.61887849A>G	GRCh38
NC_000011.9:g.61655321A>G , CM000673.1:g.61655321A>G	GRCh37
NC_000011.8:g.61411897A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000278829.7:c.213+3320T>C MANE Select	ENSP00000278829.2:n.213+3320T>C
ENST00000278829.6:c.213+3320T>C	ENSP00000278829.2:n.213+3320T>C
ENST00000414624.6:n.286+3320T>C
ENST00000525588.5:c.213+3320T>C	ENSP00000432206.1:n.213+3320T>C
ENST00000527697.5:c.-160+4010T>C	ENSP00000431533.1:n.-160+4010T>C
NM_021727.4:c.213+3320T>C	NP_068373.1:n.213+3320T>C
XM_011545023.1:c.213+3320T>C	XP_011543325.1:n.213+3320T>C
XM_011545023.2:c.213+3320T>C	XP_011543325.1:n.213+3320T>C
XM_017017723.1:c.351+4010T>C	XP_016873212.1:n.351+4010T>C
XM_017017724.1:c.351+4010T>C	XP_016873213.1:n.351+4010T>C
XR_001747866.1:n.366+4010T>C
XR_001747867.1:n.366+4010T>C
XR_001747868.1:n.377+3320T>C
XR_001747869.1:n.377+3320T>C
NM_021727.5:c.213+3320T>C MANE Select	NP_068373.1:n.213+3320T>C