Canonical Allele Identifier: CA2695170209
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154996865-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996865A>G , CM000685.2:g.154996865A>G GRCh38
NC_000023.10:g.154225140A>G , CM000685.1:g.154225140A>G GRCh37
NC_000023.9:g.153878334A>G NCBI36
NG_011403.1:g.30859T>C
NG_011403.2:g.30859T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.388+108T>C MANE Select ENSP00000353393.4:n.388+108T>C
ENST00000647125.1:c.*174+108T>C ENSP00000496062.1:n.*174+108T>C
ENST00000360256.8:c.388+108T>C ENSP00000353393.4:n.388+108T>C
ENST00000423959.5:c.283+108T>C ENSP00000409446.1:n.283+108T>C
ENST00000453950.1:c.370+108T>C ENSP00000389153.1:n.370+108T>C
NM_000132.3:c.388+108T>C NP_000123.1:n.388+108T>C
XM_011531126.1:c.283+108T>C XP_011529428.1:n.283+108T>C
NM_000132.4:c.388+108T>C MANE Select NP_000123.1:n.388+108T>C
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