Canonical Allele Identifier: CA2649037943
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586604A>C , CM000663.2:g.169586604A>C GRCh38
NC_000001.10:g.169555842A>C , CM000663.1:g.169555842A>C GRCh37
NC_000001.9:g.167822466A>C NCBI36
NG_011806.1:g.4928T>G , LRG_553:g.4928T>G

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-537T>G XP_016856149.1:n.-537T>G