Canonical Allele Identifier: CA519352699
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154124430G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896155G>A , CM000685.2:g.154896155G>A GRCh38
NC_000023.10:g.154124430G>A , CM000685.1:g.154124430G>A GRCh37
NC_000023.9:g.153777624G>A NCBI36
NG_011403.1:g.131569C>T
NG_011403.2:g.131569C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6351C>T MANE Select ENSP00000353393.4:p.Ile2117=
ENST00000360256.8:c.6351C>T ENSP00000353393.4:p.Ile2117=
NM_000132.3:c.6351C>T NP_000123.1:p.Ile2117=
XM_011531126.1:c.6246C>T XP_011529428.1:p.Ile2082=
NM_000132.4:c.6351C>T MANE Select NP_000123.1:p.Ile2117=
Search 100 bp 5'
Search 100 bp 3'