Canonical Allele Identifier: CA1234394
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs756074656

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552658A>G , CM000663.2:g.169552658A>G GRCh38
NC_000001.10:g.169521896A>G , CM000663.1:g.169521896A>G GRCh37
NC_000001.9:g.167788520A>G NCBI36
NG_011806.1:g.38874T>C , LRG_553:g.38874T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1195T>C MANE Select ENSP00000356771.3:p.Tyr399His
ENST00000367796.3:c.1195T>C ENSP00000356770.3:p.Tyr399His
ENST00000367797.7:c.1195T>C ENSP00000356771.3:p.Tyr399His
NM_000130.4:c.1195T>C , LRG_553t1:c.1195T>C NP_000121.2:p.Tyr399His
XM_017000660.2:c.784T>C XP_016856149.1:p.Tyr262His
NM_000130.5:c.1195T>C MANE Select NP_000121.2:p.Tyr399His