Canonical Allele Identifier: CA2573946651
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169555403-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555403T>C , CM000663.2:g.169555403T>C GRCh38
NC_000001.10:g.169524641T>C , CM000663.1:g.169524641T>C GRCh37
NC_000001.9:g.167791265T>C NCBI36
NG_011806.1:g.36129A>G , LRG_553:g.36129A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.953-56A>G MANE Select ENSP00000356771.3:n.953-56A>G
ENST00000367796.3:c.953-56A>G ENSP00000356770.3:n.953-56A>G
ENST00000367797.7:c.953-56A>G ENSP00000356771.3:n.953-56A>G
NM_000130.4:c.953-56A>G , LRG_553t1:c.953-56A>G NP_000121.2:n.953-56A>G
XM_017000660.2:c.542-56A>G XP_016856149.1:n.542-56A>G
NM_000130.5:c.953-56A>G MANE Select NP_000121.2:n.953-56A>G
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