Canonical Allele Identifier: CA10568654
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs781960274
ExAC: X:154250835 T / C
gnomAD v2: X-154250835-T-C
gnomAD v4: X-155022560-T-C
MyVariant Identifiers: chrX:g.154250835T>C (hg19) chrX:g.155022560T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022560T>C , CM000685.2:g.155022560T>C GRCh38
NC_000023.10:g.154250835T>C , CM000685.1:g.154250835T>C GRCh37
NC_000023.9:g.153904029T>C NCBI36
NG_011403.1:g.5164A>G
NG_011403.2:g.5164A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.-8A>G MANE Select ENSP00000353393.4:n.-8A>G
ENST00000647125.1:c.-8A>G ENSP00000496062.1:n.-8A>G
ENST00000360256.8:c.-8A>G ENSP00000353393.4:n.-8A>G
ENST00000423959.5:c.38+4220A>G ENSP00000409446.1:n.38+4220A>G
ENST00000453950.1:c.39-64A>G ENSP00000389153.1:n.39-64A>G
NM_000132.3:c.-8A>G NP_000123.1:n.-8A>G
XM_011531126.1:c.38+4220A>G XP_011529428.1:n.38+4220A>G
NM_000132.4:c.-8A>G MANE Select NP_000123.1:n.-8A>G
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