Canonical Allele Identifier: CA414913898
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156957T>A (hg19) chrX:g.154928682T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928682T>A , CM000685.2:g.154928682T>A GRCh38
NC_000023.10:g.154156957T>A , CM000685.1:g.154156957T>A GRCh37
NC_000023.9:g.153810151T>A NCBI36
NG_011403.1:g.99042A>T
NG_011403.2:g.99042A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5108A>T MANE Select ENSP00000353393.4:p.Glu1703Val
ENST00000360256.8:c.5108A>T ENSP00000353393.4:p.Glu1703Val
NM_000132.3:c.5108A>T NP_000123.1:p.Glu1703Val
XM_011531126.1:c.5003A>T XP_011529428.1:p.Glu1668Val
NM_000132.4:c.5108A>T MANE Select NP_000123.1:p.Glu1703Val
Search 100 bp 5'
Search 100 bp 3'