Canonical Allele Identifier: CA2466857712
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996802A= , CM000685.2:g.154996802A= GRCh38
NC_000023.10:g.154225077A= , CM000685.1:g.154225077A= GRCh37
NC_000023.9:g.153878271A= NCBI36
NG_011403.1:g.30922T=
NG_011403.2:g.30922T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.388+171T= MANE Select ENSP00000353393.4:n.388+171T=
ENST00000647125.1:c.*174+171T= ENSP00000496062.1:n.*174+171T=
ENST00000360256.8:c.388+171T= ENSP00000353393.4:n.388+171T=
ENST00000423959.5:c.283+171T= ENSP00000409446.1:n.283+171T=
ENST00000453950.1:c.370+171T= ENSP00000389153.1:n.370+171T=
NM_000132.3:c.388+171T= NP_000123.1:n.388+171T=
XM_011531126.1:c.283+171T= XP_011529428.1:n.283+171T=
NM_000132.4:c.388+171T= MANE Select NP_000123.1:n.388+171T=
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