Canonical Allele Identifier: CA421737956

Gene: F5

Linked Data

• dbSNP Id: rs1659548757
• gnomAD v3: 1-169529789-A-T
• gnomAD v4: 1-169529789-A-T
• MyVariant Identifiers: chr1:g.169499027A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529789A>T , CM000663.2:g.169529789A>T	GRCh38
NC_000001.10:g.169499027A>T , CM000663.1:g.169499027A>T	GRCh37
NC_000001.9:g.167765651A>T	NCBI36
NG_011806.1:g.61743T>A , LRG_553:g.61743T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5238T>A MANE Select	ENSP00000356771.3:p.Gly1746=
ENST00000367796.3:c.5253T>A	ENSP00000356770.3:p.Gly1751=
ENST00000367797.7:c.5238T>A	ENSP00000356771.3:p.Gly1746=
NM_000130.4:c.5238T>A , LRG_553t1:c.5238T>A	NP_000121.2:p.Gly1746=
XM_017000660.2:c.4827T>A	XP_016856149.1:p.Gly1609=
NM_000130.5:c.5238T>A MANE Select	NP_000121.2:p.Gly1746=