Canonical Allele Identifier: CA414913816
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2124047082
gnomAD v4: X-154928660-A-T
MyVariant Identifiers: chrX:g.154156935A>T (hg19) chrX:g.154928660A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928660A>T , CM000685.2:g.154928660A>T GRCh38
NC_000023.10:g.154156935A>T , CM000685.1:g.154156935A>T GRCh37
NC_000023.9:g.153810129A>T NCBI36
NG_011403.1:g.99064T>A
NG_011403.2:g.99064T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5130T>A MANE Select ENSP00000353393.4:p.Phe1710Leu
ENST00000360256.8:c.5130T>A ENSP00000353393.4:p.Phe1710Leu
NM_000132.3:c.5130T>A NP_000123.1:p.Phe1710Leu
XM_011531126.1:c.5025T>A XP_011529428.1:p.Phe1675Leu
NM_000132.4:c.5130T>A MANE Select NP_000123.1:p.Phe1710Leu
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