Canonical Allele Identifier: CA414917103
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154194914T>C (hg19) chrX:g.154966639T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966639T>C , CM000685.2:g.154966639T>C GRCh38
NC_000023.10:g.154194914T>C , CM000685.1:g.154194914T>C GRCh37
NC_000023.9:g.153848108T>C NCBI36
NG_011403.1:g.61085A>G
NG_011403.2:g.61085A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1058A>G MANE Select ENSP00000353393.4:p.Gln353Arg
ENST00000647125.1:c.*934A>G ENSP00000496062.1:n.*934A>G
ENST00000360256.8:c.1058A>G ENSP00000353393.4:p.Gln353Arg
NM_000132.3:c.1058A>G NP_000123.1:p.Gln353Arg
XM_011531126.1:c.953A>G XP_011529428.1:p.Gln318Arg
NM_000132.4:c.1058A>G MANE Select NP_000123.1:p.Gln353Arg
Search 100 bp 5'
Search 100 bp 3'