Canonical Allele Identifier: CA2466807439
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837681G= , CM000685.2:g.154837681G= GRCh38
NC_000023.10:g.154065956G= , CM000685.1:g.154065956G= GRCh37
NC_000023.9:g.153719150G= NCBI36
NG_011403.1:g.190043C=
NG_033065.1:g.1982C=
NG_011403.2:g.190043C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6972C= MANE Select ENSP00000353393.4:p.Tyr2324=
ENST00000644698.1:c.705C= ENSP00000495706.1:p.Tyr235=
ENST00000330287.10:c.567C= ENSP00000327895.6:p.Tyr189=
ENST00000360256.8:c.6972C= ENSP00000353393.4:p.Tyr2324=
NM_000132.3:c.6972C= NP_000123.1:p.Tyr2324=
NM_019863.2:c.567C= NP_063916.1:p.Tyr189=
XM_011531126.1:c.6867C= XP_011529428.1:p.Tyr2289=
NM_000132.4:c.6972C= MANE Select NP_000123.1:p.Tyr2324=
NM_019863.3:c.567C= NP_063916.1:p.Tyr189=