Canonical Allele Identifier: CA414904483
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154130329T>A (hg19) chrX:g.154902054T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902054T>A , CM000685.2:g.154902054T>A GRCh38
NC_000023.10:g.154130329T>A , CM000685.1:g.154130329T>A GRCh37
NC_000023.9:g.153783523T>A NCBI36
NG_011403.1:g.125670A>T
NG_011403.2:g.125670A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6112A>T MANE Select ENSP00000353393.4:p.Asn2038Tyr
ENST00000360256.8:c.6112A>T ENSP00000353393.4:p.Asn2038Tyr
NM_000132.3:c.6112A>T NP_000123.1:p.Asn2038Tyr
XM_011531126.1:c.6007A>T XP_011529428.1:p.Asn2003Tyr
NM_000132.4:c.6112A>T MANE Select NP_000123.1:p.Asn2038Tyr
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