Canonical Allele Identifier: CA2649037951
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586609A>G , CM000663.2:g.169586609A>G GRCh38
NC_000001.10:g.169555847A>G , CM000663.1:g.169555847A>G GRCh37
NC_000001.9:g.167822471A>G NCBI36
NG_011806.1:g.4923T>C , LRG_553:g.4923T>C

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-542T>C XP_016856149.1:n.-542T>C