Canonical Allele Identifier: CA10567963
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782747117
ExAC: X:154133079 T / C
gnomAD v2: X-154133079-T-C
gnomAD v4: X-154904804-T-C
MyVariant Identifiers: chrX:g.154133079T>C (hg19) chrX:g.154904804T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904804T>C , CM000685.2:g.154904804T>C GRCh38
NC_000023.10:g.154133079T>C , CM000685.1:g.154133079T>C GRCh37
NC_000023.9:g.153786273T>C NCBI36
NG_011403.1:g.122920A>G
NG_011403.2:g.122920A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5586+7A>G MANE Select ENSP00000353393.4:n.5586+7A>G
ENST00000360256.8:c.5586+7A>G ENSP00000353393.4:n.5586+7A>G
NM_000132.3:c.5586+7A>G NP_000123.1:n.5586+7A>G
XM_011531126.1:c.5481+7A>G XP_011529428.1:n.5481+7A>G
NM_000132.4:c.5586+7A>G MANE Select NP_000123.1:n.5586+7A>G
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