Canonical Allele Identifier: CA1233446
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs764069752
ExAC: 1:169495190 C / T
gnomAD v2: 1-169495190-C-T
gnomAD v4: 1-169525952-C-T
MyVariant Identifiers: chr1:g.169495190C>T (hg19) chr1:g.169525952C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525952C>T , CM000663.2:g.169525952C>T GRCh38
NC_000001.10:g.169495190C>T , CM000663.1:g.169495190C>T GRCh37
NC_000001.9:g.167761814C>T NCBI36
NG_011806.1:g.65580G>A , LRG_553:g.65580G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5665G>A MANE Select ENSP00000356771.3:p.Gly1889Arg
ENST00000367796.3:c.5680G>A ENSP00000356770.3:p.Gly1894Arg
ENST00000367797.7:c.5665G>A ENSP00000356771.3:p.Gly1889Arg
NM_000130.4:c.5665G>A , LRG_553t1:c.5665G>A NP_000121.2:p.Gly1889Arg
XM_017000660.2:c.5254G>A XP_016856149.1:p.Gly1752Arg
NM_000130.5:c.5665G>A MANE Select NP_000121.2:p.Gly1889Arg
Search 100 bp 5'
Search 100 bp 3'