Canonical Allele Identifier: CA10568602
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782288296
ExAC: X:154225355 G / A
gnomAD v2: X-154225355-G-A
gnomAD v3: X-154997080-G-A
gnomAD v4: X-154997080-G-A
MyVariant Identifiers: chrX:g.154225355G>A (hg19) chrX:g.154997080G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997080G>A , CM000685.2:g.154997080G>A GRCh38
NC_000023.10:g.154225355G>A , CM000685.1:g.154225355G>A GRCh37
NC_000023.9:g.153878549G>A NCBI36
NG_011403.1:g.30644C>T
NG_011403.2:g.30644C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.281C>T MANE Select ENSP00000353393.4:p.Thr94Ile
ENST00000647125.1:c.*67C>T ENSP00000496062.1:n.*67C>T
ENST00000360256.8:c.281C>T ENSP00000353393.4:p.Thr94Ile
ENST00000423959.5:c.176C>T ENSP00000409446.1:p.Thr59Ile
ENST00000453950.1:c.263C>T ENSP00000389153.1:p.Thr88Ile
NM_000132.3:c.281C>T NP_000123.1:p.Thr94Ile
XM_011531126.1:c.176C>T XP_011529428.1:p.Thr59Ile
NM_000132.4:c.281C>T MANE Select NP_000123.1:p.Thr94Ile
Search 100 bp 5'
Search 100 bp 3'