Canonical Allele Identifier: CA10568648
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs150495273
ExAC: X:154250759 T / C
gnomAD v2: X-154250759-T-C
gnomAD v3: X-155022484-T-C
gnomAD v4: X-155022484-T-C
MyVariant Identifiers: chrX:g.154250759T>C (hg19) chrX:g.155022484T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022484T>C , CM000685.2:g.155022484T>C GRCh38
NC_000023.10:g.154250759T>C , CM000685.1:g.154250759T>C GRCh37
NC_000023.9:g.153903953T>C NCBI36
NG_011403.1:g.5240A>G
NG_011403.2:g.5240A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.69A>G MANE Select ENSP00000353393.4:p.Arg23=
ENST00000647125.1:c.69A>G ENSP00000496062.1:p.Arg23=
ENST00000360256.8:c.69A>G ENSP00000353393.4:p.Arg23=
ENST00000423959.5:c.38+4296A>G ENSP00000409446.1:n.38+4296A>G
ENST00000453950.1:c.51A>G ENSP00000389153.1:p.Arg17=
NM_000132.3:c.69A>G NP_000123.1:p.Arg23=
XM_011531126.1:c.38+4296A>G XP_011529428.1:n.38+4296A>G
NM_000132.4:c.69A>G MANE Select NP_000123.1:p.Arg23=
Search 100 bp 5'
Search 100 bp 3'