Canonical Allele Identifier: CA519718338
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156866G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928591G>C , CM000685.2:g.154928591G>C GRCh38
NC_000023.10:g.154156866G>C , CM000685.1:g.154156866G>C GRCh37
NC_000023.9:g.153810060G>C NCBI36
NG_011403.1:g.99133C>G
NG_011403.2:g.99133C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5199C>G MANE Select ENSP00000353393.4:p.Ser1733=
ENST00000360256.8:c.5199C>G ENSP00000353393.4:p.Ser1733=
NM_000132.3:c.5199C>G NP_000123.1:p.Ser1733=
XM_011531126.1:c.5094C>G XP_011529428.1:p.Ser1698=
NM_000132.4:c.5199C>G MANE Select NP_000123.1:p.Ser1733=