Canonical Allele Identifier: CA2649037971
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586621G>T , CM000663.2:g.169586621G>T GRCh38
NC_000001.10:g.169555859G>T , CM000663.1:g.169555859G>T GRCh37
NC_000001.9:g.167822483G>T NCBI36
NG_011806.1:g.4911C>A , LRG_553:g.4911C>A

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-554C>A XP_016856149.1:n.-554C>A