Canonical Allele Identifier: CA519365979
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154194949A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966674A>T , CM000685.2:g.154966674A>T GRCh38
NC_000023.10:g.154194949A>T , CM000685.1:g.154194949A>T GRCh37
NC_000023.9:g.153848143A>T NCBI36
NG_011403.1:g.61050T>A
NG_011403.2:g.61050T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1023T>A MANE Select ENSP00000353393.4:p.Ala341=
ENST00000647125.1:c.*899T>A ENSP00000496062.1:n.*899T>A
ENST00000360256.8:c.1023T>A ENSP00000353393.4:p.Ala341=
NM_000132.3:c.1023T>A NP_000123.1:p.Ala341=
XM_011531126.1:c.918T>A XP_011529428.1:p.Ala306=
NM_000132.4:c.1023T>A MANE Select NP_000123.1:p.Ala341=
Search 100 bp 5'
Search 100 bp 3'