Canonical Allele Identifier: CA421930598

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169511001A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541763A>C , CM000663.2:g.169541763A>C	GRCh38
NC_000001.10:g.169511001A>C , CM000663.1:g.169511001A>C	GRCh37
NC_000001.9:g.167777625A>C	NCBI36
NG_011806.1:g.49769T>G , LRG_553:g.49769T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3327T>G MANE Select	ENSP00000356771.3:p.Gly1109=
ENST00000367796.3:c.3342T>G	ENSP00000356770.3:p.Gly1114=
ENST00000367797.7:c.3327T>G	ENSP00000356771.3:p.Gly1109=
NM_000130.4:c.3327T>G , LRG_553t1:c.3327T>G	NP_000121.2:p.Gly1109=
XM_017000660.2:c.2916T>G	XP_016856149.1:p.Gly972=
NM_000130.5:c.3327T>G MANE Select	NP_000121.2:p.Gly1109=