Canonical Allele Identifier: CA2649036490
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169572089-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572089C>T , CM000663.2:g.169572089C>T GRCh38
NC_000001.10:g.169541327C>T , CM000663.1:g.169541327C>T GRCh37
NC_000001.9:g.167807951C>T NCBI36
NG_011806.1:g.19443G>A , LRG_553:g.19443G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.373+132G>A MANE Select ENSP00000356771.3:n.373+132G>A
ENST00000367796.3:c.373+132G>A ENSP00000356770.3:n.373+132G>A
ENST00000367797.7:c.373+132G>A ENSP00000356771.3:n.373+132G>A
NM_000130.4:c.373+132G>A , LRG_553t1:c.373+132G>A NP_000121.2:n.373+132G>A
XM_017000660.2:c.-39+132G>A XP_016856149.1:n.-39+132G>A
NM_000130.5:c.373+132G>A MANE Select NP_000121.2:n.373+132G>A
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