Canonical Allele Identifier: CA2466844381
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154954077T= , CM000685.2:g.154954077T= GRCh38
NC_000023.10:g.154182352T= , CM000685.1:g.154182352T= GRCh37
NC_000023.9:g.153835546T= NCBI36
NG_011403.1:g.73647A=
NG_011403.2:g.73647A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1753-35A= MANE Select ENSP00000353393.4:n.1753-35A=
ENST00000647125.1:c.*1629-35A= ENSP00000496062.1:n.*1629-35A=
ENST00000360256.8:c.1753-35A= ENSP00000353393.4:n.1753-35A=
NM_000132.3:c.1753-35A= NP_000123.1:n.1753-35A=
XM_011531126.1:c.1648-35A= XP_011529428.1:n.1648-35A=
NM_000132.4:c.1753-35A= MANE Select NP_000123.1:n.1753-35A=