Canonical Allele Identifier: CA2466815679
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863206A= , CM000685.2:g.154863206A= GRCh38
NC_000023.10:g.154091481A= , CM000685.1:g.154091481A= GRCh37
NC_000023.9:g.153744675A= NCBI36
NG_011403.1:g.164518T=
NG_011403.2:g.164518T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6451T= MANE Select ENSP00000353393.4:p.Ser2151=
ENST00000644698.1:c.184T= ENSP00000495706.1:p.Ser62=
ENST00000330287.10:c.46T= ENSP00000327895.6:p.Ser16=
ENST00000360256.8:c.6451T= ENSP00000353393.4:p.Ser2151=
NM_000132.3:c.6451T= NP_000123.1:p.Ser2151=
NM_019863.2:c.46T= NP_063916.1:p.Ser16=
XM_011531126.1:c.6346T= XP_011529428.1:p.Ser2116=
NM_000132.4:c.6451T= MANE Select NP_000123.1:p.Ser2151=
NM_019863.3:c.46T= NP_063916.1:p.Ser16=