Canonical Allele Identifier: CA421930793

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169511121C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541883C>G , CM000663.2:g.169541883C>G	GRCh38
NC_000001.10:g.169511121C>G , CM000663.1:g.169511121C>G	GRCh37
NC_000001.9:g.167777745C>G	NCBI36
NG_011806.1:g.49649G>C , LRG_553:g.49649G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3207G>C MANE Select	ENSP00000356771.3:p.Val1069=
ENST00000367796.3:c.3222G>C	ENSP00000356770.3:p.Val1074=
ENST00000367797.7:c.3207G>C	ENSP00000356771.3:p.Val1069=
NM_000130.4:c.3207G>C , LRG_553t1:c.3207G>C	NP_000121.2:p.Val1069=
XM_017000660.2:c.2796G>C	XP_016856149.1:p.Val932=
NM_000130.5:c.3207G>C MANE Select	NP_000121.2:p.Val1069=