Canonical Allele Identifier: CA2649037898
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169586580-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586580G>T , CM000663.2:g.169586580G>T GRCh38
NC_000001.10:g.169555818G>T , CM000663.1:g.169555818G>T GRCh37
NC_000001.9:g.167822442G>T NCBI36
NG_011806.1:g.4952C>A , LRG_553:g.4952C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-194C>A ENSP00000356770.3:n.-194C>A
ENST00000367797.7:c.-194C>A ENSP00000356771.3:n.-194C>A
XM_017000660.2:c.-513C>A XP_016856149.1:n.-513C>A
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