Canonical Allele Identifier: CA527131367
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1320080340
gnomAD v2: 1-169555849-A-C
gnomAD v3: 1-169586611-A-C
gnomAD v4: 1-169586611-A-C
MyVariant Identifiers: chr1:g.169555849A>C (hg19) chr1:g.169586611A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586611A>C , CM000663.2:g.169586611A>C GRCh38
NC_000001.10:g.169555849A>C , CM000663.1:g.169555849A>C GRCh37
NC_000001.9:g.167822473A>C NCBI36
NG_011806.1:g.4921T>G , LRG_553:g.4921T>G

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-544T>G XP_016856149.1:n.-544T>G
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