Canonical Allele Identifier: CA2466856532
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993042T= , CM000685.2:g.154993042T= GRCh38
NC_000023.10:g.154221317T= , CM000685.1:g.154221317T= GRCh37
NC_000023.9:g.153874511T= NCBI36
NG_011403.1:g.34682A=
NG_011403.2:g.34682A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.495A= MANE Select ENSP00000353393.4:p.Pro165=
ENST00000647125.1:c.*281A= ENSP00000496062.1:n.*281A=
ENST00000360256.8:c.495A= ENSP00000353393.4:p.Pro165=
ENST00000423959.5:c.390A= ENSP00000409446.1:p.Pro130=
ENST00000453950.1:c.477A= ENSP00000389153.1:p.Pro159=
NM_000132.3:c.495A= NP_000123.1:p.Pro165=
XM_011531126.1:c.390A= XP_011529428.1:p.Pro130=
NM_000132.4:c.495A= MANE Select NP_000123.1:p.Pro165=