Canonical Allele Identifier: CA414917910
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073443163
MyVariant Identifiers: chrX:g.154197695A>G (hg19) chrX:g.154969420A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969420A>G , CM000685.2:g.154969420A>G GRCh38
NC_000023.10:g.154197695A>G , CM000685.1:g.154197695A>G GRCh37
NC_000023.9:g.153850889A>G NCBI36
NG_011403.1:g.58304T>C
NG_011403.2:g.58304T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.920T>C MANE Select ENSP00000353393.4:p.Ile307Thr
ENST00000647125.1:c.*796T>C ENSP00000496062.1:n.*796T>C
ENST00000360256.8:c.920T>C ENSP00000353393.4:p.Ile307Thr
NM_000132.3:c.920T>C NP_000123.1:p.Ile307Thr
XM_011531126.1:c.815T>C XP_011529428.1:p.Ile272Thr
NM_000132.4:c.920T>C MANE Select NP_000123.1:p.Ile307Thr
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