Canonical Allele Identifier: CA10568182
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782515887
ExAC: X:154158286 T / A
MyVariant Identifiers: chrX:g.154158286T>A (hg19) chrX:g.154930011T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154930011T>A , CM000685.2:g.154930011T>A GRCh38
NC_000023.10:g.154158286T>A , CM000685.1:g.154158286T>A GRCh37
NC_000023.9:g.153811480T>A NCBI36
NG_011403.1:g.97713A>T
NG_011403.2:g.97713A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.3779A>T MANE Select ENSP00000353393.4:p.Asp1260Val
ENST00000360256.8:c.3779A>T ENSP00000353393.4:p.Asp1260Val
NM_000132.3:c.3779A>T NP_000123.1:p.Asp1260Val
XM_011531126.1:c.3674A>T XP_011529428.1:p.Asp1225Val
NM_000132.4:c.3779A>T MANE Select NP_000123.1:p.Asp1260Val
Search 100 bp 5'
Search 100 bp 3'