Canonical Allele Identifier: CA343132676
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2856026
ClinVar RCV Id: RCV003763330
gnomAD v4: 1-169555348-C-T
MyVariant Identifiers: chr1:g.169524586C>T (hg19) chr1:g.169555348C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555348C>T , CM000663.2:g.169555348C>T GRCh38
NC_000001.10:g.169524586C>T , CM000663.1:g.169524586C>T GRCh37
NC_000001.9:g.167791210C>T NCBI36
NG_011806.1:g.36184G>A , LRG_553:g.36184G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.953-1G>A MANE Select ENSP00000356771.3:n.953-1G>A
ENST00000367796.3:c.953-1G>A ENSP00000356770.3:n.953-1G>A
ENST00000367797.7:c.953-1G>A ENSP00000356771.3:n.953-1G>A
NM_000130.4:c.953-1G>A , LRG_553t1:c.953-1G>A NP_000121.2:n.953-1G>A
XM_017000660.2:c.542-1G>A XP_016856149.1:n.542-1G>A
NM_000130.5:c.953-1G>A MANE Select NP_000121.2:n.953-1G>A
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