Canonical Allele Identifier: CA2466865397
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022390C= , CM000685.2:g.155022390C= GRCh38
NC_000023.10:g.154250665C= , CM000685.1:g.154250665C= GRCh37
NC_000023.9:g.153903859C= NCBI36
NG_011403.1:g.5334G=
NG_011403.2:g.5334G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.143+20G= MANE Select ENSP00000353393.4:n.143+20G=
ENST00000647125.1:c.121+42G= ENSP00000496062.1:n.121+42G=
ENST00000360256.8:c.143+20G= ENSP00000353393.4:n.143+20G=
ENST00000423959.5:c.38+4390G= ENSP00000409446.1:n.38+4390G=
ENST00000453950.1:c.125+20G= ENSP00000389153.1:n.125+20G=
NM_000132.3:c.143+20G= NP_000123.1:n.143+20G=
XM_011531126.1:c.38+4390G= XP_011529428.1:n.38+4390G=
NM_000132.4:c.143+20G= MANE Select NP_000123.1:n.143+20G=
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