Canonical Allele Identifier: CA645292778
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1244029338
gnomAD v2: X-154132932-G-T
gnomAD v3: X-154904657-G-T
gnomAD v4: X-154904657-G-T
MyVariant Identifiers: chrX:g.154132932G>T (hg19) chrX:g.154904657G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904657G>T , CM000685.2:g.154904657G>T GRCh38
NC_000023.10:g.154132932G>T , CM000685.1:g.154132932G>T GRCh37
NC_000023.9:g.153786126G>T NCBI36
NG_011403.1:g.123067C>A
NG_011403.2:g.123067C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5587-133C>A MANE Select ENSP00000353393.4:n.5587-133C>A
ENST00000360256.8:c.5587-133C>A ENSP00000353393.4:n.5587-133C>A
NM_000132.3:c.5587-133C>A NP_000123.1:n.5587-133C>A
XM_011531126.1:c.5482-133C>A XP_011529428.1:n.5482-133C>A
NM_000132.4:c.5587-133C>A MANE Select NP_000123.1:n.5587-133C>A
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