Canonical Allele Identifier: CA2466827601
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154901997C= , CM000685.2:g.154901997C= GRCh38
NC_000023.10:g.154130272C= , CM000685.1:g.154130272C= GRCh37
NC_000023.9:g.153783466C= NCBI36
NG_011403.1:g.125727G=
NG_011403.2:g.125727G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6115+54G= MANE Select ENSP00000353393.4:n.6115+54G=
ENST00000360256.8:c.6115+54G= ENSP00000353393.4:n.6115+54G=
NM_000132.3:c.6115+54G= NP_000123.1:n.6115+54G=
XM_011531126.1:c.6010+54G= XP_011529428.1:n.6010+54G=
NM_000132.4:c.6115+54G= MANE Select NP_000123.1:n.6115+54G=
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