Canonical Allele Identifier: CA343132083
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1660292767

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555302G>C , CM000663.2:g.169555302G>C GRCh38
NC_000001.10:g.169524540G>C , CM000663.1:g.169524540G>C GRCh37
NC_000001.9:g.167791164G>C NCBI36
NG_011806.1:g.36230C>G , LRG_553:g.36230C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.998C>G MANE Select ENSP00000356771.3:p.Thr333Ser
ENST00000367796.3:c.998C>G ENSP00000356770.3:p.Thr333Ser
ENST00000367797.7:c.998C>G ENSP00000356771.3:p.Thr333Ser
NM_000130.4:c.998C>G , LRG_553t1:c.998C>G NP_000121.2:p.Thr333Ser
XM_017000660.2:c.587C>G XP_016856149.1:p.Thr196Ser
NM_000130.5:c.998C>G MANE Select NP_000121.2:p.Thr333Ser