Canonical Allele Identifier: CA2649037757
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586502G>A , CM000663.2:g.169586502G>A GRCh38
NC_000001.10:g.169555740G>A , CM000663.1:g.169555740G>A GRCh37
NC_000001.9:g.167822364G>A NCBI36
NG_011806.1:g.5030C>T , LRG_553:g.5030C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-116C>T ENSP00000356770.3:n.-116C>T
ENST00000367797.7:c.-116C>T ENSP00000356771.3:n.-116C>T
NM_000130.4:c.-116C>T , LRG_553t1:c.-116C>T NP_000121.2:n.-116C>T
XM_017000660.2:c.-435C>T XP_016856149.1:n.-435C>T