Canonical Allele Identifier: CA2524105615
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572556T>A , CM000663.2:g.169572556T>A GRCh38
NC_000001.10:g.169541794T>A , CM000663.1:g.169541794T>A GRCh37
NC_000001.9:g.167808418T>A NCBI36
NG_011806.1:g.18976A>T , LRG_553:g.18976A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-213A>T MANE Select ENSP00000356771.3:n.251-213A>T
ENST00000367796.3:c.251-213A>T ENSP00000356770.3:n.251-213A>T
ENST00000367797.7:c.251-213A>T ENSP00000356771.3:n.251-213A>T
NM_000130.4:c.251-213A>T , LRG_553t1:c.251-213A>T NP_000121.2:n.251-213A>T
XM_017000660.2:c.-161-213A>T XP_016856149.1:n.-161-213A>T
NM_000130.5:c.251-213A>T MANE Select NP_000121.2:n.251-213A>T