Canonical Allele Identifier: CA2574085087

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529838T>C , CM000663.2:g.169529838T>C	GRCh38
NC_000001.10:g.169499076T>C , CM000663.1:g.169499076T>C	GRCh37
NC_000001.9:g.167765700T>C	NCBI36
NG_011806.1:g.61694A>G , LRG_553:g.61694A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5209-20A>G MANE Select	ENSP00000356771.3:n.5209-20A>G
ENST00000367796.3:c.5224-20A>G	ENSP00000356770.3:n.5224-20A>G
ENST00000367797.7:c.5209-20A>G	ENSP00000356771.3:n.5209-20A>G
NM_000130.4:c.5209-20A>G , LRG_553t1:c.5209-20A>G	NP_000121.2:n.5209-20A>G
XM_017000660.2:c.4798-20A>G	XP_016856149.1:n.4798-20A>G
NM_000130.5:c.5209-20A>G MANE Select	NP_000121.2:n.5209-20A>G