Canonical Allele Identifier: CA519719949
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154159740A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931465A>G , CM000685.2:g.154931465A>G GRCh38
NC_000023.10:g.154159740A>G , CM000685.1:g.154159740A>G GRCh37
NC_000023.9:g.153812934A>G NCBI36
NG_011403.1:g.96259T>C
NG_011403.2:g.96259T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2325T>C MANE Select ENSP00000353393.4:p.Phe775=
ENST00000647125.1:c.*1991T>C ENSP00000496062.1:n.*1991T>C
ENST00000360256.8:c.2325T>C ENSP00000353393.4:p.Phe775=
NM_000132.3:c.2325T>C NP_000123.1:p.Phe775=
XM_011531126.1:c.2220T>C XP_011529428.1:p.Phe740=
NM_000132.4:c.2325T>C MANE Select NP_000123.1:p.Phe775=
Search 100 bp 5'
Search 100 bp 3'