Canonical Allele Identifier: CA343124548

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169495146C>G (hg19) ; chr1:g.169525908C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525908C>G , CM000663.2:g.169525908C>G	GRCh38
NC_000001.10:g.169495146C>G , CM000663.1:g.169495146C>G	GRCh37
NC_000001.9:g.167761770C>G	NCBI36
NG_011806.1:g.65624G>C , LRG_553:g.65624G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5709G>C MANE Select	ENSP00000356771.3:p.Met1903Ile
ENST00000367796.3:c.5724G>C	ENSP00000356770.3:p.Met1908Ile
ENST00000367797.7:c.5709G>C	ENSP00000356771.3:p.Met1903Ile
NM_000130.4:c.5709G>C , LRG_553t1:c.5709G>C	NP_000121.2:p.Met1903Ile
XM_017000660.2:c.5298G>C	XP_016856149.1:p.Met1766Ile
NM_000130.5:c.5709G>C MANE Select	NP_000121.2:p.Met1903Ile