Canonical Allele Identifier: CA2466865381
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022364C= , CM000685.2:g.155022364C= GRCh38
NC_000023.10:g.154250639C= , CM000685.1:g.154250639C= GRCh37
NC_000023.9:g.153903833C= NCBI36
NG_011403.1:g.5360G=
NG_011403.2:g.5360G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.143+46G= MANE Select ENSP00000353393.4:n.143+46G=
ENST00000647125.1:c.121+68G= ENSP00000496062.1:n.121+68G=
ENST00000360256.8:c.143+46G= ENSP00000353393.4:n.143+46G=
ENST00000423959.5:c.38+4416G= ENSP00000409446.1:n.38+4416G=
ENST00000453950.1:c.125+46G= ENSP00000389153.1:n.125+46G=
NM_000132.3:c.143+46G= NP_000123.1:n.143+46G=
XM_011531126.1:c.38+4416G= XP_011529428.1:n.38+4416G=
NM_000132.4:c.143+46G= MANE Select NP_000123.1:n.143+46G=
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