Canonical Allele Identifier: CA1206156999
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs541336863

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586596G>A , CM000663.2:g.169586596G>A GRCh38
NC_000001.10:g.169555834G>A , CM000663.1:g.169555834G>A GRCh37
NC_000001.9:g.167822458G>A NCBI36
NG_011806.1:g.4936C>T , LRG_553:g.4936C>T

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-529C>T XP_016856149.1:n.-529C>T