Canonical Allele Identifier: CA2466828166
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904008T= , CM000685.2:g.154904008T= GRCh38
NC_000023.10:g.154132283T= , CM000685.1:g.154132283T= GRCh37
NC_000023.9:g.153785477T= NCBI36
NG_011403.1:g.123716A=
NG_011403.2:g.123716A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5896A= MANE Select ENSP00000353393.4:p.Met1966=
ENST00000360256.8:c.5896A= ENSP00000353393.4:p.Met1966=
NM_000132.3:c.5896A= NP_000123.1:p.Met1966=
XM_011531126.1:c.5791A= XP_011529428.1:p.Met1931=
NM_000132.4:c.5896A= MANE Select NP_000123.1:p.Met1966=