Canonical Allele Identifier: CA2466815676
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863205G= , CM000685.2:g.154863205G= GRCh38
NC_000023.10:g.154091480G= , CM000685.1:g.154091480G= GRCh37
NC_000023.9:g.153744674G= NCBI36
NG_011403.1:g.164519C=
NG_011403.2:g.164519C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6452C= MANE Select ENSP00000353393.4:p.Ser2151=
ENST00000644698.1:c.185C= ENSP00000495706.1:p.Ser62=
ENST00000330287.10:c.47C= ENSP00000327895.6:p.Ser16=
ENST00000360256.8:c.6452C= ENSP00000353393.4:p.Ser2151=
NM_000132.3:c.6452C= NP_000123.1:p.Ser2151=
NM_019863.2:c.47C= NP_063916.1:p.Ser16=
XM_011531126.1:c.6347C= XP_011529428.1:p.Ser2116=
NM_000132.4:c.6452C= MANE Select NP_000123.1:p.Ser2151=
NM_019863.3:c.47C= NP_063916.1:p.Ser16=