Canonical Allele Identifier: CA2649037966
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169586618-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586618A>G , CM000663.2:g.169586618A>G GRCh38
NC_000001.10:g.169555856A>G , CM000663.1:g.169555856A>G GRCh37
NC_000001.9:g.167822480A>G NCBI36
NG_011806.1:g.4914T>C , LRG_553:g.4914T>C

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-551T>C XP_016856149.1:n.-551T>C
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