Canonical Allele Identifier: CA10567930
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782244803
ExAC: X:154132350 G / A
gnomAD v4: X-154904075-G-A
MyVariant Identifiers: chrX:g.154132350G>A (hg19) chrX:g.154904075G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904075G>A , CM000685.2:g.154904075G>A GRCh38
NC_000023.10:g.154132350G>A , CM000685.1:g.154132350G>A GRCh37
NC_000023.9:g.153785544G>A NCBI36
NG_011403.1:g.123649C>T
NG_011403.2:g.123649C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5829C>T MANE Select ENSP00000353393.4:p.Tyr1943=
ENST00000360256.8:c.5829C>T ENSP00000353393.4:p.Tyr1943=
NM_000132.3:c.5829C>T NP_000123.1:p.Tyr1943=
XM_011531126.1:c.5724C>T XP_011529428.1:p.Tyr1908=
NM_000132.4:c.5829C>T MANE Select NP_000123.1:p.Tyr1943=
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