Canonical Allele Identifier: CA2746577842

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549604C>T , CM000663.2:g.169549604C>T	GRCh38
NC_000001.10:g.169518842C>T , CM000663.1:g.169518842C>T	GRCh37
NC_000001.9:g.167785466C>T	NCBI36
NG_011806.1:g.41928G>A , LRG_553:g.41928G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1611+197G>A MANE Select	ENSP00000356771.3:n.1611+197G>A
ENST00000367796.3:c.1611+197G>A	ENSP00000356770.3:n.1611+197G>A
ENST00000367797.7:c.1611+197G>A	ENSP00000356771.3:n.1611+197G>A
NM_000130.4:c.1611+197G>A , LRG_553t1:c.1611+197G>A	NP_000121.2:n.1611+197G>A
XM_017000660.2:c.1200+197G>A	XP_016856149.1:n.1200+197G>A
NM_000130.5:c.1611+197G>A MANE Select	NP_000121.2:n.1611+197G>A