Canonical Allele Identifier: CA32418352
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs982657792
gnomAD v3: 1-169586629-G-T
gnomAD v4: 1-169586629-G-T
MyVariant Identifiers: chr1:g.169555867G>T (hg19) chr1:g.169586629G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586629G>T , CM000663.2:g.169586629G>T GRCh38
NC_000001.10:g.169555867G>T , CM000663.1:g.169555867G>T GRCh37
NC_000001.9:g.167822491G>T NCBI36
NG_011806.1:g.4903C>A , LRG_553:g.4903C>A

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-562C>A XP_016856149.1:n.-562C>A
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