Canonical Allele Identifier: CA2649036587
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169555387-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555387A>G , CM000663.2:g.169555387A>G GRCh38
NC_000001.10:g.169524625A>G , CM000663.1:g.169524625A>G GRCh37
NC_000001.9:g.167791249A>G NCBI36
NG_011806.1:g.36145T>C , LRG_553:g.36145T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.953-40T>C MANE Select ENSP00000356771.3:n.953-40T>C
ENST00000367796.3:c.953-40T>C ENSP00000356770.3:n.953-40T>C
ENST00000367797.7:c.953-40T>C ENSP00000356771.3:n.953-40T>C
NM_000130.4:c.953-40T>C , LRG_553t1:c.953-40T>C NP_000121.2:n.953-40T>C
XM_017000660.2:c.542-40T>C XP_016856149.1:n.542-40T>C
NM_000130.5:c.953-40T>C MANE Select NP_000121.2:n.953-40T>C
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