Canonical Allele Identifier: CA2649037922
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169586591-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586591C>A , CM000663.2:g.169586591C>A GRCh38
NC_000001.10:g.169555829C>A , CM000663.1:g.169555829C>A GRCh37
NC_000001.9:g.167822453C>A NCBI36
NG_011806.1:g.4941G>T , LRG_553:g.4941G>T

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-524G>T XP_016856149.1:n.-524G>T
Search 100 bp 5'
Search 100 bp 3'