Canonical Allele Identifier: CA343118570
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541777A>G , CM000663.2:g.169541777A>G GRCh38
NC_000001.10:g.169511015A>G , CM000663.1:g.169511015A>G GRCh37
NC_000001.9:g.167777639A>G NCBI36
NG_011806.1:g.49755T>C , LRG_553:g.49755T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.3313T>C MANE Select ENSP00000356771.3:p.Ser1105Pro
ENST00000367796.3:c.3328T>C ENSP00000356770.3:p.Ser1110Pro
ENST00000367797.7:c.3313T>C ENSP00000356771.3:p.Ser1105Pro
NM_000130.4:c.3313T>C , LRG_553t1:c.3313T>C NP_000121.2:p.Ser1105Pro
XM_017000660.2:c.2902T>C XP_016856149.1:p.Ser968Pro
NM_000130.5:c.3313T>C MANE Select NP_000121.2:p.Ser1105Pro