Canonical Allele Identifier: CA519374745
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156863T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928588T>A , CM000685.2:g.154928588T>A GRCh38
NC_000023.10:g.154156863T>A , CM000685.1:g.154156863T>A GRCh37
NC_000023.9:g.153810057T>A NCBI36
NG_011403.1:g.99136A>T
NG_011403.2:g.99136A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5202A>T MANE Select ENSP00000353393.4:p.Pro1734=
ENST00000360256.8:c.5202A>T ENSP00000353393.4:p.Pro1734=
NM_000132.3:c.5202A>T NP_000123.1:p.Pro1734=
XM_011531126.1:c.5097A>T XP_011529428.1:p.Pro1699=
NM_000132.4:c.5202A>T MANE Select NP_000123.1:p.Pro1734=
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