Canonical Allele Identifier: CA2695152814
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154901935-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154901935G>T , CM000685.2:g.154901935G>T GRCh38
NC_000023.10:g.154130210G>T , CM000685.1:g.154130210G>T GRCh37
NC_000023.9:g.153783404G>T NCBI36
NG_011403.1:g.125789C>A
NG_011403.2:g.125789C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6115+116C>A MANE Select ENSP00000353393.4:n.6115+116C>A
ENST00000360256.8:c.6115+116C>A ENSP00000353393.4:n.6115+116C>A
NM_000132.3:c.6115+116C>A NP_000123.1:n.6115+116C>A
XM_011531126.1:c.6010+116C>A XP_011529428.1:n.6010+116C>A
NM_000132.4:c.6115+116C>A MANE Select NP_000123.1:n.6115+116C>A
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