Canonical Allele Identifier: CA519718457
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157085T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928810T>G , CM000685.2:g.154928810T>G GRCh38
NC_000023.10:g.154157085T>G , CM000685.1:g.154157085T>G GRCh37
NC_000023.9:g.153810279T>G NCBI36
NG_011403.1:g.98914A>C
NG_011403.2:g.98914A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4980A>C MANE Select ENSP00000353393.4:p.Pro1660=
ENST00000360256.8:c.4980A>C ENSP00000353393.4:p.Pro1660=
NM_000132.3:c.4980A>C NP_000123.1:p.Pro1660=
XM_011531126.1:c.4875A>C XP_011529428.1:p.Pro1625=
NM_000132.4:c.4980A>C MANE Select NP_000123.1:p.Pro1660=