Canonical Allele Identifier: CA1206148808
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1337264283
gnomAD v4: 1-169572434-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572434G>T , CM000663.2:g.169572434G>T GRCh38
NC_000001.10:g.169541672G>T , CM000663.1:g.169541672G>T GRCh37
NC_000001.9:g.167808296G>T NCBI36
NG_011806.1:g.19098C>A , LRG_553:g.19098C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-91C>A MANE Select ENSP00000356771.3:n.251-91C>A
ENST00000367796.3:c.251-91C>A ENSP00000356770.3:n.251-91C>A
ENST00000367797.7:c.251-91C>A ENSP00000356771.3:n.251-91C>A
NM_000130.4:c.251-91C>A , LRG_553t1:c.251-91C>A NP_000121.2:n.251-91C>A
XM_017000660.2:c.-161-91C>A XP_016856149.1:n.-161-91C>A
NM_000130.5:c.251-91C>A MANE Select NP_000121.2:n.251-91C>A
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