Canonical Allele Identifier: CA1206156998
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1661110658

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586593G>C , CM000663.2:g.169586593G>C GRCh38
NC_000001.10:g.169555831G>C , CM000663.1:g.169555831G>C GRCh37
NC_000001.9:g.167822455G>C NCBI36
NG_011806.1:g.4939C>G , LRG_553:g.4939C>G

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-526C>G XP_016856149.1:n.-526C>G