Canonical Allele Identifier: CA414915497
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157186G>A (hg19) chrX:g.154928911G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928911G>A , CM000685.2:g.154928911G>A GRCh38
NC_000023.10:g.154157186G>A , CM000685.1:g.154157186G>A GRCh37
NC_000023.9:g.153810380G>A NCBI36
NG_011403.1:g.98813C>T
NG_011403.2:g.98813C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4879C>T MANE Select ENSP00000353393.4:p.His1627Tyr
ENST00000360256.8:c.4879C>T ENSP00000353393.4:p.His1627Tyr
NM_000132.3:c.4879C>T NP_000123.1:p.His1627Tyr
XM_011531126.1:c.4774C>T XP_011529428.1:p.His1592Tyr
NM_000132.4:c.4879C>T MANE Select NP_000123.1:p.His1627Tyr
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