Canonical Allele Identifier: CA2573946662

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555417T>G , CM000663.2:g.169555417T>G	GRCh38
NC_000001.10:g.169524655T>G , CM000663.1:g.169524655T>G	GRCh37
NC_000001.9:g.167791279T>G	NCBI36
NG_011806.1:g.36115A>C , LRG_553:g.36115A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.953-70A>C MANE Select	ENSP00000356771.3:n.953-70A>C
ENST00000367796.3:c.953-70A>C	ENSP00000356770.3:n.953-70A>C
ENST00000367797.7:c.953-70A>C	ENSP00000356771.3:n.953-70A>C
NM_000130.4:c.953-70A>C , LRG_553t1:c.953-70A>C	NP_000121.2:n.953-70A>C
XM_017000660.2:c.542-70A>C	XP_016856149.1:n.542-70A>C
NM_000130.5:c.953-70A>C MANE Select	NP_000121.2:n.953-70A>C