Canonical Allele Identifier: CA2466845293
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956931C= , CM000685.2:g.154956931C= GRCh38
NC_000023.10:g.154185206C= , CM000685.1:g.154185206C= GRCh37
NC_000023.9:g.153838400C= NCBI36
NG_011403.1:g.70793G=
NG_011403.2:g.70793G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1752+26G= MANE Select ENSP00000353393.4:n.1752+26G=
ENST00000647125.1:c.*1628+26G= ENSP00000496062.1:n.*1628+26G=
ENST00000360256.8:c.1752+26G= ENSP00000353393.4:n.1752+26G=
NM_000132.3:c.1752+26G= NP_000123.1:n.1752+26G=
XM_011531126.1:c.1647+26G= XP_011529428.1:n.1647+26G=
NM_000132.4:c.1752+26G= MANE Select NP_000123.1:n.1752+26G=