Canonical Allele Identifier: CA32390640
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs902441840

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555301G>C , CM000663.2:g.169555301G>C GRCh38
NC_000001.10:g.169524539G>C , CM000663.1:g.169524539G>C GRCh37
NC_000001.9:g.167791163G>C NCBI36
NG_011806.1:g.36231C>G , LRG_553:g.36231C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.999C>G MANE Select ENSP00000356771.3:p.Thr333=
ENST00000367796.3:c.999C>G ENSP00000356770.3:p.Thr333=
ENST00000367797.7:c.999C>G ENSP00000356771.3:p.Thr333=
NM_000130.4:c.999C>G , LRG_553t1:c.999C>G NP_000121.2:p.Thr333=
XM_017000660.2:c.588C>G XP_016856149.1:p.Thr196=
NM_000130.5:c.999C>G MANE Select NP_000121.2:p.Thr333=