Canonical Allele Identifier: CA1234464
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs541800681

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555357G>A , CM000663.2:g.169555357G>A GRCh38
NC_000001.10:g.169524595G>A , CM000663.1:g.169524595G>A GRCh37
NC_000001.9:g.167791219G>A NCBI36
NG_011806.1:g.36175C>T , LRG_553:g.36175C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.953-10C>T MANE Select ENSP00000356771.3:n.953-10C>T
ENST00000367796.3:c.953-10C>T ENSP00000356770.3:n.953-10C>T
ENST00000367797.7:c.953-10C>T ENSP00000356771.3:n.953-10C>T
NM_000130.4:c.953-10C>T , LRG_553t1:c.953-10C>T NP_000121.2:n.953-10C>T
XM_017000660.2:c.542-10C>T XP_016856149.1:n.542-10C>T
NM_000130.5:c.953-10C>T MANE Select NP_000121.2:n.953-10C>T