Canonical Allele Identifier: CA519717853
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132305C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904030C>T , CM000685.2:g.154904030C>T GRCh38
NC_000023.10:g.154132305C>T , CM000685.1:g.154132305C>T GRCh37
NC_000023.9:g.153785499C>T NCBI36
NG_011403.1:g.123694G>A
NG_011403.2:g.123694G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5874G>A MANE Select ENSP00000353393.4:p.Arg1958=
ENST00000360256.8:c.5874G>A ENSP00000353393.4:p.Arg1958=
NM_000132.3:c.5874G>A NP_000123.1:p.Arg1958=
XM_011531126.1:c.5769G>A XP_011529428.1:p.Arg1923=
NM_000132.4:c.5874G>A MANE Select NP_000123.1:p.Arg1958=