Canonical Allele Identifier: CA32390569
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1054956664
gnomAD v2: 1-169524454-C-T
gnomAD v4: 1-169555216-C-T
MyVariant Identifiers: chr1:g.169524454C>T (hg19) chr1:g.169555216C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555216C>T , CM000663.2:g.169555216C>T GRCh38
NC_000001.10:g.169524454C>T , CM000663.1:g.169524454C>T GRCh37
NC_000001.9:g.167791078C>T NCBI36
NG_011806.1:g.36316G>A , LRG_553:g.36316G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1084G>A MANE Select ENSP00000356771.3:p.Asp362Asn
ENST00000367796.3:c.1084G>A ENSP00000356770.3:p.Asp362Asn
ENST00000367797.7:c.1084G>A ENSP00000356771.3:p.Asp362Asn
NM_000130.4:c.1084G>A , LRG_553t1:c.1084G>A NP_000121.2:p.Asp362Asn
XM_017000660.2:c.673G>A XP_016856149.1:p.Asp225Asn
NM_000130.5:c.1084G>A MANE Select NP_000121.2:p.Asp362Asn
Search 100 bp 5'
Search 100 bp 3'