Canonical Allele Identifier: CA2649037916
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169586587-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586587C>T , CM000663.2:g.169586587C>T GRCh38
NC_000001.10:g.169555825C>T , CM000663.1:g.169555825C>T GRCh37
NC_000001.9:g.167822449C>T NCBI36
NG_011806.1:g.4945G>A , LRG_553:g.4945G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-201G>A ENSP00000356770.3:n.-201G>A
ENST00000367797.7:c.-201G>A ENSP00000356771.3:n.-201G>A
XM_017000660.2:c.-520G>A XP_016856149.1:n.-520G>A
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