Canonical Allele Identifier: CA414908899
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1377219599

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904976G>C , CM000685.2:g.154904976G>C GRCh38
NC_000023.10:g.154133251G>C , CM000685.1:g.154133251G>C GRCh37
NC_000023.9:g.153786445G>C NCBI36
NG_011403.1:g.122748C>G
NG_011403.2:g.122748C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5421C>G MANE Select ENSP00000353393.4:p.Ser1807Arg
ENST00000360256.8:c.5421C>G ENSP00000353393.4:p.Ser1807Arg
NM_000132.3:c.5421C>G NP_000123.1:p.Ser1807Arg
XM_011531126.1:c.5316C>G XP_011529428.1:p.Ser1772Arg
NM_000132.4:c.5421C>G MANE Select NP_000123.1:p.Ser1807Arg