Canonical Allele Identifier: CA414913907
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156959A>T (hg19) chrX:g.154928684A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928684A>T , CM000685.2:g.154928684A>T GRCh38
NC_000023.10:g.154156959A>T , CM000685.1:g.154156959A>T GRCh37
NC_000023.9:g.153810153A>T NCBI36
NG_011403.1:g.99040T>A
NG_011403.2:g.99040T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5106T>A MANE Select ENSP00000353393.4:p.Asp1702Glu
ENST00000360256.8:c.5106T>A ENSP00000353393.4:p.Asp1702Glu
NM_000132.3:c.5106T>A NP_000123.1:p.Asp1702Glu
XM_011531126.1:c.5001T>A XP_011529428.1:p.Asp1667Glu
NM_000132.4:c.5106T>A MANE Select NP_000123.1:p.Asp1702Glu
Search 100 bp 5'
Search 100 bp 3'