Canonical Allele Identifier: CA1008987210
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1660750328

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572562G>C , CM000663.2:g.169572562G>C GRCh38
NC_000001.10:g.169541800G>C , CM000663.1:g.169541800G>C GRCh37
NC_000001.9:g.167808424G>C NCBI36
NG_011806.1:g.18970C>G , LRG_553:g.18970C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-219C>G MANE Select ENSP00000356771.3:n.251-219C>G
ENST00000367796.3:c.251-219C>G ENSP00000356770.3:n.251-219C>G
ENST00000367797.7:c.251-219C>G ENSP00000356771.3:n.251-219C>G
NM_000130.4:c.251-219C>G , LRG_553t1:c.251-219C>G NP_000121.2:n.251-219C>G
XM_017000660.2:c.-161-219C>G XP_016856149.1:n.-161-219C>G
NM_000130.5:c.251-219C>G MANE Select NP_000121.2:n.251-219C>G