Canonical Allele Identifier: CA1233780
Gene: F5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 37345
dbSNP Id: rs1800595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541110T>C , CM000663.2:g.169541110T>C GRCh38
NC_000001.10:g.169510348T>C , CM000663.1:g.169510348T>C GRCh37
NC_000001.9:g.167776972T>C NCBI36
NG_011806.1:g.50422A>G , LRG_553:g.50422A>G

Transcript Alleles

HGVS Amino-acid change
NM_000130.4:c.3980A>G , LRG_553t1:c.3980A>G NP_000121.2:p.His1327Arg
XM_017000660.2:c.3569A>G XP_016856149.1:p.His1190Arg
ENST00000367796.3:c.3995A>G ENSP00000356770.3:p.His1332Arg
ENST00000367797.7:c.3980A>G ENSP00000356771.3:p.His1327Arg