Canonical Allele Identifier: CA873341422
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1159427333
gnomAD v3: X-154905055-C-G
gnomAD v4: X-154905055-C-G
MyVariant Identifiers: chrX:g.154905055C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905055C>G , CM000685.2:g.154905055C>G GRCh38
NC_000023.10:g.154133330C>G , CM000685.1:g.154133330C>G GRCh37
NC_000023.9:g.153786524C>G NCBI36
NG_011403.1:g.122669G>C
NG_011403.2:g.122669G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5374-32G>C MANE Select ENSP00000353393.4:n.5374-32G>C
ENST00000360256.8:c.5374-32G>C ENSP00000353393.4:n.5374-32G>C
NM_000132.3:c.5374-32G>C NP_000123.1:n.5374-32G>C
XM_011531126.1:c.5269-32G>C XP_011529428.1:n.5269-32G>C
NM_000132.4:c.5374-32G>C MANE Select NP_000123.1:n.5374-32G>C
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