Canonical Allele Identifier: CA1206157001
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1571608780
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586597T>G , CM000663.2:g.169586597T>G GRCh38
NC_000001.10:g.169555835T>G , CM000663.1:g.169555835T>G GRCh37
NC_000001.9:g.167822459T>G NCBI36
NG_011806.1:g.4935A>C , LRG_553:g.4935A>C

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-530A>C XP_016856149.1:n.-530A>C
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