Canonical Allele Identifier: CA414914843
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157117T>A (hg19) chrX:g.154928842T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928842T>A , CM000685.2:g.154928842T>A GRCh38
NC_000023.10:g.154157117T>A , CM000685.1:g.154157117T>A GRCh37
NC_000023.9:g.153810311T>A NCBI36
NG_011403.1:g.98882A>T
NG_011403.2:g.98882A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4948A>T MANE Select ENSP00000353393.4:p.Arg1650Trp
ENST00000360256.8:c.4948A>T ENSP00000353393.4:p.Arg1650Trp
NM_000132.3:c.4948A>T NP_000123.1:p.Arg1650Trp
XM_011531126.1:c.4843A>T XP_011529428.1:p.Arg1615Trp
NM_000132.4:c.4948A>T MANE Select NP_000123.1:p.Arg1650Trp
Search 100 bp 5'
Search 100 bp 3'