Canonical Allele Identifier: CA414908976
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs137852444
MyVariant Identifiers: chrX:g.154133264G>A (hg19) chrX:g.154904989G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904989G>A , CM000685.2:g.154904989G>A GRCh38
NC_000023.10:g.154133264G>A , CM000685.1:g.154133264G>A GRCh37
NC_000023.9:g.153786458G>A NCBI36
NG_011403.1:g.122735C>T
NG_011403.2:g.122735C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5408C>T MANE Select ENSP00000353393.4:p.Ser1803Phe
ENST00000360256.8:c.5408C>T ENSP00000353393.4:p.Ser1803Phe
NM_000132.3:c.5408C>T NP_000123.1:p.Ser1803Phe
XM_011531126.1:c.5303C>T XP_011529428.1:p.Ser1768Phe
NM_000132.4:c.5408C>T MANE Select NP_000123.1:p.Ser1803Phe
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