Canonical Allele Identifier: CA414914229
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157029T>A (hg19) chrX:g.154928754T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928754T>A , CM000685.2:g.154928754T>A GRCh38
NC_000023.10:g.154157029T>A , CM000685.1:g.154157029T>A GRCh37
NC_000023.9:g.153810223T>A NCBI36
NG_011403.1:g.98970A>T
NG_011403.2:g.98970A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5036A>T MANE Select ENSP00000353393.4:p.Glu1679Val
ENST00000360256.8:c.5036A>T ENSP00000353393.4:p.Glu1679Val
NM_000132.3:c.5036A>T NP_000123.1:p.Glu1679Val
XM_011531126.1:c.4931A>T XP_011529428.1:p.Glu1644Val
NM_000132.4:c.5036A>T MANE Select NP_000123.1:p.Glu1679Val
Search 100 bp 5'
Search 100 bp 3'