Canonical Allele Identifier: CA890946171
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1448136852
gnomAD v3: 1-169586506-G-T
gnomAD v4: 1-169586506-G-T
MyVariant Identifiers: chr1:g.169555744G>T (hg19) chr1:g.169586506G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586506G>T , CM000663.2:g.169586506G>T GRCh38
NC_000001.10:g.169555744G>T , CM000663.1:g.169555744G>T GRCh37
NC_000001.9:g.167822368G>T NCBI36
NG_011806.1:g.5026C>A , LRG_553:g.5026C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-120C>A ENSP00000356770.3:n.-120C>A
ENST00000367797.7:c.-120C>A ENSP00000356771.3:n.-120C>A
NM_000130.4:c.-120C>A , LRG_553t1:c.-120C>A NP_000121.2:n.-120C>A
XM_017000660.2:c.-439C>A XP_016856149.1:n.-439C>A
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