Canonical Allele Identifier: CA414910526
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1557280941
gnomAD v2: X-154182202-T-A
gnomAD v4: X-154953927-T-A
MyVariant Identifiers: chrX:g.154182202T>A (hg19) chrX:g.154953927T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953927T>A , CM000685.2:g.154953927T>A GRCh38
NC_000023.10:g.154182202T>A , CM000685.1:g.154182202T>A GRCh37
NC_000023.9:g.153835396T>A NCBI36
NG_011403.1:g.73797A>T
NG_011403.2:g.73797A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1868A>T MANE Select ENSP00000353393.4:p.Glu623Val
ENST00000647125.1:c.*1744A>T ENSP00000496062.1:n.*1744A>T
ENST00000360256.8:c.1868A>T ENSP00000353393.4:p.Glu623Val
NM_000132.3:c.1868A>T NP_000123.1:p.Glu623Val
XM_011531126.1:c.1763A>T XP_011529428.1:p.Glu588Val
NM_000132.4:c.1868A>T MANE Select NP_000123.1:p.Glu623Val
Search 100 bp 5'
Search 100 bp 3'