Canonical Allele Identifier: CA2649037961
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586615C>A , CM000663.2:g.169586615C>A GRCh38
NC_000001.10:g.169555853C>A , CM000663.1:g.169555853C>A GRCh37
NC_000001.9:g.167822477C>A NCBI36
NG_011806.1:g.4917G>T , LRG_553:g.4917G>T

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-548G>T XP_016856149.1:n.-548G>T