Canonical Allele Identifier: CA10568399
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs137852424
ExAC: X:154182266 G / T
gnomAD v2: X-154182266-G-T
gnomAD v4: X-154953991-G-T
MyVariant Identifiers: chrX:g.154182266G>T (hg19) chrX:g.154953991G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953991G>T , CM000685.2:g.154953991G>T GRCh38
NC_000023.10:g.154182266G>T , CM000685.1:g.154182266G>T GRCh37
NC_000023.9:g.153835460G>T NCBI36
NG_011403.1:g.73733C>A
NG_011403.2:g.73733C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1804C>A MANE Select ENSP00000353393.4:p.Arg602=
ENST00000647125.1:c.*1680C>A ENSP00000496062.1:n.*1680C>A
ENST00000360256.8:c.1804C>A ENSP00000353393.4:p.Arg602=
NM_000132.3:c.1804C>A NP_000123.1:p.Arg602=
XM_011531126.1:c.1699C>A XP_011529428.1:p.Arg567=
NM_000132.4:c.1804C>A MANE Select NP_000123.1:p.Arg602=
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