Canonical Allele Identifier: CA2649035742

Gene: F5

Linked Data

• gnomAD v4: 1-169530660-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169530660C>A , CM000663.2:g.169530660C>A	GRCh38
NC_000001.10:g.169499898C>A , CM000663.1:g.169499898C>A	GRCh37
NC_000001.9:g.167766522C>A	NCBI36
NG_011806.1:g.60872G>T , LRG_553:g.60872G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5208+126G>T MANE Select	ENSP00000356771.3:n.5208+126G>T
ENST00000367796.3:c.5223+126G>T	ENSP00000356770.3:n.5223+126G>T
ENST00000367797.7:c.5208+126G>T	ENSP00000356771.3:n.5208+126G>T
NM_000130.4:c.5208+126G>T , LRG_553t1:c.5208+126G>T	NP_000121.2:n.5208+126G>T
XM_017000660.2:c.4797+126G>T	XP_016856149.1:n.4797+126G>T
NM_000130.5:c.5208+126G>T MANE Select	NP_000121.2:n.5208+126G>T