Canonical Allele Identifier: CA337336620
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs137852370

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966655A>G , CM000685.2:g.154966655A>G GRCh38
NC_000023.10:g.154194930A>G , CM000685.1:g.154194930A>G GRCh37
NC_000023.9:g.153848124A>G NCBI36
NG_011403.1:g.61069T>C
NG_011403.2:g.61069T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1042T>C MANE Select ENSP00000353393.4:p.Cys348Arg
ENST00000647125.1:c.*918T>C ENSP00000496062.1:p.=
ENST00000360256.8:c.1042T>C ENSP00000353393.4:p.Cys348Arg
NM_000132.3:c.1042T>C NP_000123.1:p.Cys348Arg
XM_011531126.1:c.937T>C XP_011529428.1:p.Cys313Arg
NM_000132.4:c.1042T>C MANE Select NP_000123.1:p.Cys348Arg