Canonical Allele Identifier: CA519374732
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156847T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928572T>G , CM000685.2:g.154928572T>G GRCh38
NC_000023.10:g.154156847T>G , CM000685.1:g.154156847T>G GRCh37
NC_000023.9:g.153810041T>G NCBI36
NG_011403.1:g.99152A>C
NG_011403.2:g.99152A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5218A>C MANE Select ENSP00000353393.4:p.Arg1740=
ENST00000360256.8:c.5218A>C ENSP00000353393.4:p.Arg1740=
NM_000132.3:c.5218A>C NP_000123.1:p.Arg1740=
XM_011531126.1:c.5113A>C XP_011529428.1:p.Arg1705=
NM_000132.4:c.5218A>C MANE Select NP_000123.1:p.Arg1740=