Canonical Allele Identifier: CA519352702
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154896155-G-T
MyVariant Identifiers: chrX:g.154124430G>T (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6351C>A MANE Select ENSP00000353393.4:p.Ile2117=
ENST00000360256.8:c.6351C>A ENSP00000353393.4:p.Ile2117=
NM_000132.3:c.6351C>A NP_000123.1:p.Ile2117=
XM_011531126.1:c.6246C>A XP_011529428.1:p.Ile2082=
NM_000132.4:c.6351C>A MANE Select NP_000123.1:p.Ile2117=
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