Canonical Allele Identifier: CA2649037907
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169586583-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586583T>C , CM000663.2:g.169586583T>C GRCh38
NC_000001.10:g.169555821T>C , CM000663.1:g.169555821T>C GRCh37
NC_000001.9:g.167822445T>C NCBI36
NG_011806.1:g.4949A>G , LRG_553:g.4949A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-197A>G ENSP00000356770.3:n.-197A>G
ENST00000367797.7:c.-197A>G ENSP00000356771.3:n.-197A>G
XM_017000660.2:c.-516A>G XP_016856149.1:n.-516A>G
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