Canonical Allele Identifier: CA645251840
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1281938076
gnomAD v2: X-154130313-C-G
MyVariant Identifiers: chrX:g.154130313C>G (hg19) chrX:g.154902038C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902038C>G , CM000685.2:g.154902038C>G GRCh38
NC_000023.10:g.154130313C>G , CM000685.1:g.154130313C>G GRCh37
NC_000023.9:g.153783507C>G NCBI36
NG_011403.1:g.125686G>C
NG_011403.2:g.125686G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6115+13G>C MANE Select ENSP00000353393.4:n.6115+13G>C
ENST00000360256.8:c.6115+13G>C ENSP00000353393.4:n.6115+13G>C
NM_000132.3:c.6115+13G>C NP_000123.1:n.6115+13G>C
XM_011531126.1:c.6010+13G>C XP_011529428.1:n.6010+13G>C
NM_000132.4:c.6115+13G>C MANE Select NP_000123.1:n.6115+13G>C
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