Canonical Allele Identifier: CA10568649
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs375887989
ExAC: X:154250777 G / A
gnomAD v2: X-154250777-G-A
gnomAD v3: X-155022502-G-A
gnomAD v4: X-155022502-G-A
MyVariant Identifiers: chrX:g.154250777G>A (hg19) chrX:g.155022502G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022502G>A , CM000685.2:g.155022502G>A GRCh38
NC_000023.10:g.154250777G>A , CM000685.1:g.154250777G>A GRCh37
NC_000023.9:g.153903971G>A NCBI36
NG_011403.1:g.5222C>T
NG_011403.2:g.5222C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.51C>T MANE Select ENSP00000353393.4:p.Cys17=
ENST00000647125.1:c.51C>T ENSP00000496062.1:p.Cys17=
ENST00000360256.8:c.51C>T ENSP00000353393.4:p.Cys17=
ENST00000423959.5:c.38+4278C>T ENSP00000409446.1:n.38+4278C>T
ENST00000453950.1:c.39-6C>T ENSP00000389153.1:n.39-6C>T
NM_000132.3:c.51C>T NP_000123.1:p.Cys17=
XM_011531126.1:c.38+4278C>T XP_011529428.1:n.38+4278C>T
NM_000132.4:c.51C>T MANE Select NP_000123.1:p.Cys17=
Search 100 bp 5'
Search 100 bp 3'