Canonical Allele Identifier: CA414918192
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154197758T>G (hg19) chrX:g.154969483T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969483T>G , CM000685.2:g.154969483T>G GRCh38
NC_000023.10:g.154197758T>G , CM000685.1:g.154197758T>G GRCh37
NC_000023.9:g.153850952T>G NCBI36
NG_011403.1:g.58241A>C
NG_011403.2:g.58241A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.857A>C MANE Select ENSP00000353393.4:p.His286Pro
ENST00000647125.1:c.*733A>C ENSP00000496062.1:n.*733A>C
ENST00000360256.8:c.857A>C ENSP00000353393.4:p.His286Pro
NM_000132.3:c.857A>C NP_000123.1:p.His286Pro
XM_011531126.1:c.752A>C XP_011529428.1:p.His251Pro
NM_000132.4:c.857A>C MANE Select NP_000123.1:p.His286Pro
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