Canonical Allele Identifier: CA414920577
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073765013
MyVariant Identifiers: chrX:g.154250753G>C (hg19) chrX:g.155022478G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022478G>C , CM000685.2:g.155022478G>C GRCh38
NC_000023.10:g.154250753G>C , CM000685.1:g.154250753G>C GRCh37
NC_000023.9:g.153903947G>C NCBI36
NG_011403.1:g.5246C>G
NG_011403.2:g.5246C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.75C>G MANE Select ENSP00000353393.4:p.Tyr25Ter
ENST00000647125.1:c.75C>G ENSP00000496062.1:p.Tyr25Ter
ENST00000360256.8:c.75C>G ENSP00000353393.4:p.Tyr25Ter
ENST00000423959.5:c.38+4302C>G ENSP00000409446.1:n.38+4302C>G
ENST00000453950.1:c.57C>G ENSP00000389153.1:p.Tyr19Ter
NM_000132.3:c.75C>G NP_000123.1:p.Tyr25Ter
XM_011531126.1:c.38+4302C>G XP_011529428.1:n.38+4302C>G
NM_000132.4:c.75C>G MANE Select NP_000123.1:p.Tyr25Ter
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