Canonical Allele Identifier: CA414918121
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154197741C>T (hg19) chrX:g.154969466C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969466C>T , CM000685.2:g.154969466C>T GRCh38
NC_000023.10:g.154197741C>T , CM000685.1:g.154197741C>T GRCh37
NC_000023.9:g.153850935C>T NCBI36
NG_011403.1:g.58258G>A
NG_011403.2:g.58258G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.874G>A MANE Select ENSP00000353393.4:p.Gly292Ser
ENST00000647125.1:c.*750G>A ENSP00000496062.1:n.*750G>A
ENST00000360256.8:c.874G>A ENSP00000353393.4:p.Gly292Ser
NM_000132.3:c.874G>A NP_000123.1:p.Gly292Ser
XM_011531126.1:c.769G>A XP_011529428.1:p.Gly257Ser
NM_000132.4:c.874G>A MANE Select NP_000123.1:p.Gly292Ser
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