Canonical Allele Identifier: CA2649036176
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552815A>T , CM000663.2:g.169552815A>T GRCh38
NC_000001.10:g.169522053A>T , CM000663.1:g.169522053A>T GRCh37
NC_000001.9:g.167788677A>T NCBI36
NG_011806.1:g.38717T>A , LRG_553:g.38717T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1119-81T>A MANE Select ENSP00000356771.3:n.1119-81T>A
ENST00000367796.3:c.1119-81T>A ENSP00000356770.3:n.1119-81T>A
ENST00000367797.7:c.1119-81T>A ENSP00000356771.3:n.1119-81T>A
NM_000130.4:c.1119-81T>A , LRG_553t1:c.1119-81T>A NP_000121.2:n.1119-81T>A
XM_017000660.2:c.708-81T>A XP_016856149.1:n.708-81T>A
NM_000130.5:c.1119-81T>A MANE Select NP_000121.2:n.1119-81T>A