Canonical Allele Identifier: CA2466807431
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837660A= , CM000685.2:g.154837660A= GRCh38
NC_000023.10:g.154065935A= , CM000685.1:g.154065935A= GRCh37
NC_000023.9:g.153719129A= NCBI36
NG_011403.1:g.190064T=
NG_033065.1:g.2003T=
NG_011403.2:g.190064T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6993T= MANE Select ENSP00000353393.4:p.Ser2331=
ENST00000644698.1:c.726T= ENSP00000495706.1:p.Ser242=
ENST00000330287.10:c.588T= ENSP00000327895.6:p.Ser196=
ENST00000360256.8:c.6993T= ENSP00000353393.4:p.Ser2331=
NM_000132.3:c.6993T= NP_000123.1:p.Ser2331=
NM_019863.2:c.588T= NP_063916.1:p.Ser196=
XM_011531126.1:c.6888T= XP_011529428.1:p.Ser2296=
NM_000132.4:c.6993T= MANE Select NP_000123.1:p.Ser2331=
NM_019863.3:c.588T= NP_063916.1:p.Ser196=