Canonical Allele Identifier: CA2649037904
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169586582-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586582T>A , CM000663.2:g.169586582T>A GRCh38
NC_000001.10:g.169555820T>A , CM000663.1:g.169555820T>A GRCh37
NC_000001.9:g.167822444T>A NCBI36
NG_011806.1:g.4950A>T , LRG_553:g.4950A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-196A>T ENSP00000356770.3:n.-196A>T
ENST00000367797.7:c.-196A>T ENSP00000356771.3:n.-196A>T
XM_017000660.2:c.-515A>T XP_016856149.1:n.-515A>T
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