Canonical Allele Identifier: CA2466828389
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904738A= , CM000685.2:g.154904738A= GRCh38
NC_000023.10:g.154133013A= , CM000685.1:g.154133013A= GRCh37
NC_000023.9:g.153786207A= NCBI36
NG_011403.1:g.122986T=
NG_011403.2:g.122986T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5586+73T= MANE Select ENSP00000353393.4:n.5586+73T=
ENST00000360256.8:c.5586+73T= ENSP00000353393.4:n.5586+73T=
NM_000132.3:c.5586+73T= NP_000123.1:n.5586+73T=
XM_011531126.1:c.5481+73T= XP_011529428.1:n.5481+73T=
NM_000132.4:c.5586+73T= MANE Select NP_000123.1:n.5586+73T=