Canonical Allele Identifier: CA414913533
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156874T>A (hg19) chrX:g.154928599T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928599T>A , CM000685.2:g.154928599T>A GRCh38
NC_000023.10:g.154156874T>A , CM000685.1:g.154156874T>A GRCh37
NC_000023.9:g.153810068T>A NCBI36
NG_011403.1:g.99125A>T
NG_011403.2:g.99125A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5191A>T MANE Select ENSP00000353393.4:p.Ser1731Cys
ENST00000360256.8:c.5191A>T ENSP00000353393.4:p.Ser1731Cys
NM_000132.3:c.5191A>T NP_000123.1:p.Ser1731Cys
XM_011531126.1:c.5086A>T XP_011529428.1:p.Ser1696Cys
NM_000132.4:c.5191A>T MANE Select NP_000123.1:p.Ser1731Cys
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