Canonical Allele Identifier: CA414909224
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154176035T>A (hg19) chrX:g.154947760T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154947760T>A , CM000685.2:g.154947760T>A GRCh38
NC_000023.10:g.154176035T>A , CM000685.1:g.154176035T>A GRCh37
NC_000023.9:g.153829229T>A NCBI36
NG_011403.1:g.79964A>T
NG_011403.2:g.79964A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.2051A>T MANE Select ENSP00000353393.4:p.Glu684Val
ENST00000647125.1:c.*1779+6132A>T ENSP00000496062.1:n.*1779+6132A>T
ENST00000360256.8:c.2051A>T ENSP00000353393.4:p.Glu684Val
NM_000132.3:c.2051A>T NP_000123.1:p.Glu684Val
XM_011531126.1:c.1946A>T XP_011529428.1:p.Glu649Val
NM_000132.4:c.2051A>T MANE Select NP_000123.1:p.Glu684Val
Search 100 bp 5'
Search 100 bp 3'