Canonical Allele Identifier: CA2466836205
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154930003A= , CM000685.2:g.154930003A= GRCh38
NC_000023.10:g.154158278A= , CM000685.1:g.154158278A= GRCh37
NC_000023.9:g.153811472A= NCBI36
NG_011403.1:g.97721T=
NG_011403.2:g.97721T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.3787T= MANE Select ENSP00000353393.4:p.Tyr1263=
ENST00000360256.8:c.3787T= ENSP00000353393.4:p.Tyr1263=
NM_000132.3:c.3787T= NP_000123.1:p.Tyr1263=
XM_011531126.1:c.3682T= XP_011529428.1:p.Tyr1228=
NM_000132.4:c.3787T= MANE Select NP_000123.1:p.Tyr1263=