Canonical Allele Identifier: CA32425917

Gene: F5

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169522862T>G , CM000663.2:g.169522862T>G	GRCh38
NC_000001.10:g.169492100T>G , CM000663.1:g.169492100T>G	GRCh37
NC_000001.9:g.167758724T>G	NCBI36
NG_011806.1:g.68670A>C , LRG_553:g.68670A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.6048+335A>C MANE Select	ENSP00000356771.3:n.6048+335A>C
ENST00000367796.3:c.6063+335A>C	ENSP00000356770.3:n.6063+335A>C
ENST00000367797.7:c.6048+335A>C	ENSP00000356771.3:n.6048+335A>C
NM_000130.4:c.6048+335A>C , LRG_553t1:c.6048+335A>C	NP_000121.2:n.6048+335A>C
XM_017000660.2:c.5637+335A>C	XP_016856149.1:n.5637+335A>C
NM_000130.5:c.6048+335A>C MANE Select	NP_000121.2:n.6048+335A>C