Canonical Allele Identifier: CA873356880
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1452973446
gnomAD v3: X-154965925-A-T
gnomAD v4: X-154965925-A-T
MyVariant Identifiers: chrX:g.154965925A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154965925A>T , CM000685.2:g.154965925A>T GRCh38
NC_000023.10:g.154194200A>T , CM000685.1:g.154194200A>T GRCh37
NC_000023.9:g.153847394A>T NCBI36
NG_011403.1:g.61799T>A
NG_011403.2:g.61799T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1443+45T>A MANE Select ENSP00000353393.4:n.1443+45T>A
ENST00000647125.1:c.*1319+45T>A ENSP00000496062.1:n.*1319+45T>A
ENST00000360256.8:c.1443+45T>A ENSP00000353393.4:n.1443+45T>A
ENST00000483822.2:n.308T>A
NM_000132.3:c.1443+45T>A NP_000123.1:n.1443+45T>A
XM_011531126.1:c.1338+45T>A XP_011529428.1:n.1338+45T>A
NM_000132.4:c.1443+45T>A MANE Select NP_000123.1:n.1443+45T>A
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