Canonical Allele Identifier: CA414902514
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154931507-G-T
MyVariant Identifiers: chrX:g.154159782G>T (hg19) chrX:g.154931507G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931507G>T , CM000685.2:g.154931507G>T GRCh38
NC_000023.10:g.154159782G>T , CM000685.1:g.154159782G>T GRCh37
NC_000023.9:g.153812976G>T NCBI36
NG_011403.1:g.96217C>A
NG_011403.2:g.96217C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2283C>A MANE Select ENSP00000353393.4:p.Phe761Leu
ENST00000647125.1:c.*1949C>A ENSP00000496062.1:n.*1949C>A
ENST00000360256.8:c.2283C>A ENSP00000353393.4:p.Phe761Leu
NM_000132.3:c.2283C>A NP_000123.1:p.Phe761Leu
XM_011531126.1:c.2178C>A XP_011529428.1:p.Phe726Leu
NM_000132.4:c.2283C>A MANE Select NP_000123.1:p.Phe761Leu
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