Canonical Allele Identifier: CA414905825
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs137852451
MyVariant Identifiers: chrX:g.154132241G>C (hg19) chrX:g.154903966G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903966G>C , CM000685.2:g.154903966G>C GRCh38
NC_000023.10:g.154132241G>C , CM000685.1:g.154132241G>C GRCh37
NC_000023.9:g.153785435G>C NCBI36
NG_011403.1:g.123758C>G
NG_011403.2:g.123758C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5938C>G MANE Select ENSP00000353393.4:p.His1980Asp
ENST00000360256.8:c.5938C>G ENSP00000353393.4:p.His1980Asp
NM_000132.3:c.5938C>G NP_000123.1:p.His1980Asp
XM_011531126.1:c.5833C>G XP_011529428.1:p.His1945Asp
NM_000132.4:c.5938C>G MANE Select NP_000123.1:p.His1980Asp
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