Canonical Allele Identifier: CA873339935
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1467726860
gnomAD v3: X-154901939-A-C
gnomAD v4: X-154901939-A-C
MyVariant Identifiers: chrX:g.154901939A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154901939A>C , CM000685.2:g.154901939A>C GRCh38
NC_000023.10:g.154130214A>C , CM000685.1:g.154130214A>C GRCh37
NC_000023.9:g.153783408A>C NCBI36
NG_011403.1:g.125785T>G
NG_011403.2:g.125785T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6115+112T>G MANE Select ENSP00000353393.4:n.6115+112T>G
ENST00000360256.8:c.6115+112T>G ENSP00000353393.4:n.6115+112T>G
NM_000132.3:c.6115+112T>G NP_000123.1:n.6115+112T>G
XM_011531126.1:c.6010+112T>G XP_011529428.1:n.6010+112T>G
NM_000132.4:c.6115+112T>G MANE Select NP_000123.1:n.6115+112T>G
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