Canonical Allele Identifier: CA2466865489
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022663C= , CM000685.2:g.155022663C= GRCh38
NC_000023.10:g.154250938C= , CM000685.1:g.154250938C= GRCh37
NC_000023.9:g.153904132C= NCBI36
NG_011403.1:g.5061G=
NG_011403.2:g.5061G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.-111G= MANE Select ENSP00000353393.4:n.-111G=
ENST00000647125.1:c.-111G= ENSP00000496062.1:n.-111G=
ENST00000360256.8:c.-111G= ENSP00000353393.4:n.-111G=
ENST00000423959.5:c.38+4117G= ENSP00000409446.1:n.38+4117G=
ENST00000453950.1:c.39-167G= ENSP00000389153.1:n.39-167G=
NM_000132.3:c.-111G= NP_000123.1:n.-111G=
XM_011531126.1:c.38+4117G= XP_011529428.1:n.38+4117G=
NM_000132.4:c.-111G= MANE Select NP_000123.1:n.-111G=
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