Canonical Allele Identifier: CA414910670
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953943C>G , CM000685.2:g.154953943C>G GRCh38
NC_000023.10:g.154182218C>G , CM000685.1:g.154182218C>G GRCh37
NC_000023.9:g.153835412C>G NCBI36
NG_011403.1:g.73781G>C
NG_011403.2:g.73781G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1852G>C MANE Select ENSP00000353393.4:p.Ala618Pro
ENST00000647125.1:c.*1728G>C ENSP00000496062.1:n.*1728G>C
ENST00000360256.8:c.1852G>C ENSP00000353393.4:p.Ala618Pro
NM_000132.3:c.1852G>C NP_000123.1:p.Ala618Pro
XM_011531126.1:c.1747G>C XP_011529428.1:p.Ala583Pro
NM_000132.4:c.1852G>C MANE Select NP_000123.1:p.Ala618Pro