Canonical Allele Identifier: CA414918441
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154197815C>G (hg19) chrX:g.154969540C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969540C>G , CM000685.2:g.154969540C>G GRCh38
NC_000023.10:g.154197815C>G , CM000685.1:g.154197815C>G GRCh37
NC_000023.9:g.153851009C>G NCBI36
NG_011403.1:g.58184G>C
NG_011403.2:g.58184G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.800G>C MANE Select ENSP00000353393.4:p.Cys267Ser
ENST00000647125.1:c.*676G>C ENSP00000496062.1:n.*676G>C
ENST00000360256.8:c.800G>C ENSP00000353393.4:p.Cys267Ser
NM_000132.3:c.800G>C NP_000123.1:p.Cys267Ser
XM_011531126.1:c.695G>C XP_011529428.1:p.Cys232Ser
NM_000132.4:c.800G>C MANE Select NP_000123.1:p.Cys267Ser
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