Canonical Allele Identifier: CA343118005
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1659855465
gnomAD v3: 1-169541677-A-C
gnomAD v4: 1-169541677-A-C
MyVariant Identifiers: chr1:g.169510915A>C (hg19) chr1:g.169541677A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541677A>C , CM000663.2:g.169541677A>C GRCh38
NC_000001.10:g.169510915A>C , CM000663.1:g.169510915A>C GRCh37
NC_000001.9:g.167777539A>C NCBI36
NG_011806.1:g.49855T>G , LRG_553:g.49855T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.3413T>G MANE Select ENSP00000356771.3:p.Met1138Arg
ENST00000367796.3:c.3428T>G ENSP00000356770.3:p.Met1143Arg
ENST00000367797.7:c.3413T>G ENSP00000356771.3:p.Met1138Arg
NM_000130.4:c.3413T>G , LRG_553t1:c.3413T>G NP_000121.2:p.Met1138Arg
XM_017000660.2:c.3002T>G XP_016856149.1:p.Met1001Arg
NM_000130.5:c.3413T>G MANE Select NP_000121.2:p.Met1138Arg
Search 100 bp 5'
Search 100 bp 3'