Canonical Allele Identifier: CA337332801
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1054449581
MyVariant Identifiers: chrX:g.154956913T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956913T>A , CM000685.2:g.154956913T>A GRCh38
NC_000023.10:g.154185188T>A , CM000685.1:g.154185188T>A GRCh37
NC_000023.9:g.153838382T>A NCBI36
NG_011403.1:g.70811A>T
NG_011403.2:g.70811A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1752+44A>T MANE Select ENSP00000353393.4:n.1752+44A>T
ENST00000647125.1:c.*1628+44A>T ENSP00000496062.1:n.*1628+44A>T
ENST00000360256.8:c.1752+44A>T ENSP00000353393.4:n.1752+44A>T
NM_000132.3:c.1752+44A>T NP_000123.1:n.1752+44A>T
XM_011531126.1:c.1647+44A>T XP_011529428.1:n.1647+44A>T
NM_000132.4:c.1752+44A>T MANE Select NP_000123.1:n.1752+44A>T
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