Canonical Allele Identifier: CA337318585
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1032356229
gnomAD v3: X-154904668-G-A
gnomAD v4: X-154904668-G-A
MyVariant Identifiers: chrX:g.154904668G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904668G>A , CM000685.2:g.154904668G>A GRCh38
NC_000023.10:g.154132943G>A , CM000685.1:g.154132943G>A GRCh37
NC_000023.9:g.153786137G>A NCBI36
NG_011403.1:g.123056C>T
NG_011403.2:g.123056C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5587-144C>T MANE Select ENSP00000353393.4:n.5587-144C>T
ENST00000360256.8:c.5587-144C>T ENSP00000353393.4:n.5587-144C>T
NM_000132.3:c.5587-144C>T NP_000123.1:n.5587-144C>T
XM_011531126.1:c.5482-144C>T XP_011529428.1:n.5482-144C>T
NM_000132.4:c.5587-144C>T MANE Select NP_000123.1:n.5587-144C>T
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