Canonical Allele Identifier: CA2466815612
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863115A= , CM000685.2:g.154863115A= GRCh38
NC_000023.10:g.154091390A= , CM000685.1:g.154091390A= GRCh37
NC_000023.9:g.153744584A= NCBI36
NG_011403.1:g.164609T=
NG_011403.2:g.164609T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6542T= MANE Select ENSP00000353393.4:p.Leu2181=
ENST00000644698.1:c.275T= ENSP00000495706.1:p.Leu92=
ENST00000330287.10:c.137T= ENSP00000327895.6:p.Leu46=
ENST00000360256.8:c.6542T= ENSP00000353393.4:p.Leu2181=
NM_000132.3:c.6542T= NP_000123.1:p.Leu2181=
NM_019863.2:c.137T= NP_063916.1:p.Leu46=
XM_011531126.1:c.6437T= XP_011529428.1:p.Leu2146=
NM_000132.4:c.6542T= MANE Select NP_000123.1:p.Leu2181=
NM_019863.3:c.137T= NP_063916.1:p.Leu46=