Canonical Allele Identifier: CA519357273
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1603432997
gnomAD v3: X-154904904-G-A
gnomAD v4: X-154904904-G-A
MyVariant Identifiers: chrX:g.154133179G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904904G>A , CM000685.2:g.154904904G>A GRCh38
NC_000023.10:g.154133179G>A , CM000685.1:g.154133179G>A GRCh37
NC_000023.9:g.153786373G>A NCBI36
NG_011403.1:g.122820C>T
NG_011403.2:g.122820C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5493C>T MANE Select ENSP00000353393.4:p.Thr1831=
ENST00000360256.8:c.5493C>T ENSP00000353393.4:p.Thr1831=
NM_000132.3:c.5493C>T NP_000123.1:p.Thr1831=
XM_011531126.1:c.5388C>T XP_011529428.1:p.Thr1796=
NM_000132.4:c.5493C>T MANE Select NP_000123.1:p.Thr1831=
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