Canonical Allele Identifier: CA343130943
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1660285000

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555203A>C , CM000663.2:g.169555203A>C GRCh38
NC_000001.10:g.169524441A>C , CM000663.1:g.169524441A>C GRCh37
NC_000001.9:g.167791065A>C NCBI36
NG_011806.1:g.36329T>G , LRG_553:g.36329T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.1097T>G MANE Select ENSP00000356771.3:p.Val366Gly
ENST00000367796.3:c.1097T>G ENSP00000356770.3:p.Val366Gly
ENST00000367797.7:c.1097T>G ENSP00000356771.3:p.Val366Gly
NM_000130.4:c.1097T>G , LRG_553t1:c.1097T>G NP_000121.2:p.Val366Gly
XM_017000660.2:c.686T>G XP_016856149.1:p.Val229Gly
NM_000130.5:c.1097T>G MANE Select NP_000121.2:p.Val366Gly