Canonical Allele Identifier: CA414908550
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154133127A>C (hg19) chrX:g.154904852A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904852A>C , CM000685.2:g.154904852A>C GRCh38
NC_000023.10:g.154133127A>C , CM000685.1:g.154133127A>C GRCh37
NC_000023.9:g.153786321A>C NCBI36
NG_011403.1:g.122872T>G
NG_011403.2:g.122872T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5545T>G MANE Select ENSP00000353393.4:p.Phe1849Val
ENST00000360256.8:c.5545T>G ENSP00000353393.4:p.Phe1849Val
NM_000132.3:c.5545T>G NP_000123.1:p.Phe1849Val
XM_011531126.1:c.5440T>G XP_011529428.1:p.Phe1814Val
NM_000132.4:c.5545T>G MANE Select NP_000123.1:p.Phe1849Val
Search 100 bp 5'
Search 100 bp 3'