Canonical Allele Identifier: CA890946170
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1171045247
gnomAD v4: 1-169586497-T-C
MyVariant Identifiers: chr1:g.169555735T>C (hg19) chr1:g.169586497T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586497T>C , CM000663.2:g.169586497T>C GRCh38
NC_000001.10:g.169555735T>C , CM000663.1:g.169555735T>C GRCh37
NC_000001.9:g.167822359T>C NCBI36
NG_011806.1:g.5035A>G , LRG_553:g.5035A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-111A>G ENSP00000356770.3:n.-111A>G
ENST00000367797.7:c.-111A>G ENSP00000356771.3:n.-111A>G
NM_000130.4:c.-111A>G , LRG_553t1:c.-111A>G NP_000121.2:n.-111A>G
XM_017000660.2:c.-430A>G XP_016856149.1:n.-430A>G
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