Canonical Allele Identifier: CA2466827603
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902014G= , CM000685.2:g.154902014G= GRCh38
NC_000023.10:g.154130289G= , CM000685.1:g.154130289G= GRCh37
NC_000023.9:g.153783483G= NCBI36
NG_011403.1:g.125710C=
NG_011403.2:g.125710C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6115+37C= MANE Select ENSP00000353393.4:n.6115+37C=
ENST00000360256.8:c.6115+37C= ENSP00000353393.4:n.6115+37C=
NM_000132.3:c.6115+37C= NP_000123.1:n.6115+37C=
XM_011531126.1:c.6010+37C= XP_011529428.1:n.6010+37C=
NM_000132.4:c.6115+37C= MANE Select NP_000123.1:n.6115+37C=
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