Canonical Allele Identifier: CA2649037970
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169586619-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586619G>T , CM000663.2:g.169586619G>T GRCh38
NC_000001.10:g.169555857G>T , CM000663.1:g.169555857G>T GRCh37
NC_000001.9:g.167822481G>T NCBI36
NG_011806.1:g.4913C>A , LRG_553:g.4913C>A

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-552C>A XP_016856149.1:n.-552C>A
Search 100 bp 5'
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