Canonical Allele Identifier: CA343117898

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169510891T>G (hg19) ; chr1:g.169541653T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541653T>G , CM000663.2:g.169541653T>G	GRCh38
NC_000001.10:g.169510891T>G , CM000663.1:g.169510891T>G	GRCh37
NC_000001.9:g.167777515T>G	NCBI36
NG_011806.1:g.49879A>C , LRG_553:g.49879A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3437A>C MANE Select	ENSP00000356771.3:p.His1146Pro
ENST00000367796.3:c.3452A>C	ENSP00000356770.3:p.His1151Pro
ENST00000367797.7:c.3437A>C	ENSP00000356771.3:p.His1146Pro
NM_000130.4:c.3437A>C , LRG_553t1:c.3437A>C	NP_000121.2:p.His1146Pro
XM_017000660.2:c.3026A>C	XP_016856149.1:p.His1009Pro
NM_000130.5:c.3437A>C MANE Select	NP_000121.2:p.His1146Pro