Canonical Allele Identifier: CA2466857734
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996897G= , CM000685.2:g.154996897G= GRCh38
NC_000023.10:g.154225172G= , CM000685.1:g.154225172G= GRCh37
NC_000023.9:g.153878366G= NCBI36
NG_011403.1:g.30827C=
NG_011403.2:g.30827C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.388+76C= MANE Select ENSP00000353393.4:n.388+76C=
ENST00000647125.1:c.*174+76C= ENSP00000496062.1:n.*174+76C=
ENST00000360256.8:c.388+76C= ENSP00000353393.4:n.388+76C=
ENST00000423959.5:c.283+76C= ENSP00000409446.1:n.283+76C=
ENST00000453950.1:c.370+76C= ENSP00000389153.1:n.370+76C=
NM_000132.3:c.388+76C= NP_000123.1:n.388+76C=
XM_011531126.1:c.283+76C= XP_011529428.1:n.283+76C=
NM_000132.4:c.388+76C= MANE Select NP_000123.1:n.388+76C=
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