Canonical Allele Identifier: CA255170
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10281
dbSNP Id: rs28933675

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904867G>A , CM000685.2:g.154904867G>A GRCh38
NC_000023.10:g.154133142G>A , CM000685.1:g.154133142G>A GRCh37
NC_000023.9:g.153786336G>A NCBI36
NG_011403.1:g.122857C>T
NG_011403.2:g.122857C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5530C>T MANE Select ENSP00000353393.4:p.Pro1844Ser
ENST00000360256.8:c.5530C>T ENSP00000353393.4:p.Pro1844Ser
NM_000132.3:c.5530C>T NP_000123.1:p.Pro1844Ser
XM_011531126.1:c.5425C>T XP_011529428.1:p.Pro1809Ser
NM_000132.4:c.5530C>T MANE Select NP_000123.1:p.Pro1844Ser