Canonical Allele Identifier: CA343124905

Gene: F5

Linked Data

• gnomAD v4: 1-169525955-C-A
• MyVariant Identifiers: chr1:g.169495193C>A (hg19) ; chr1:g.169525955C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525955C>A , CM000663.2:g.169525955C>A	GRCh38
NC_000001.10:g.169495193C>A , CM000663.1:g.169495193C>A	GRCh37
NC_000001.9:g.167761817C>A	NCBI36
NG_011806.1:g.65577G>T , LRG_553:g.65577G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5662G>T MANE Select	ENSP00000356771.3:p.Val1888Phe
ENST00000367796.3:c.5677G>T	ENSP00000356770.3:p.Val1893Phe
ENST00000367797.7:c.5662G>T	ENSP00000356771.3:p.Val1888Phe
NM_000130.4:c.5662G>T , LRG_553t1:c.5662G>T	NP_000121.2:p.Val1888Phe
XM_017000660.2:c.5251G>T	XP_016856149.1:p.Val1751Phe
NM_000130.5:c.5662G>T MANE Select	NP_000121.2:p.Val1888Phe