Canonical Allele Identifier: CA2466828196
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904085A= , CM000685.2:g.154904085A= GRCh38
NC_000023.10:g.154132360A= , CM000685.1:g.154132360A= GRCh37
NC_000023.9:g.153785554A= NCBI36
NG_011403.1:g.123639T=
NG_011403.2:g.123639T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5819T= MANE Select ENSP00000353393.4:p.Ile1940=
ENST00000360256.8:c.5819T= ENSP00000353393.4:p.Ile1940=
NM_000132.3:c.5819T= NP_000123.1:p.Ile1940=
XM_011531126.1:c.5714T= XP_011529428.1:p.Ile1905=
NM_000132.4:c.5819T= MANE Select NP_000123.1:p.Ile1940=