Canonical Allele Identifier: CA414908632
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154133151G>C (hg19) chrX:g.154904876G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904876G>C , CM000685.2:g.154904876G>C GRCh38
NC_000023.10:g.154133151G>C , CM000685.1:g.154133151G>C GRCh37
NC_000023.9:g.153786345G>C NCBI36
NG_011403.1:g.122848C>G
NG_011403.2:g.122848C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5521C>G MANE Select ENSP00000353393.4:p.His1841Asp
ENST00000360256.8:c.5521C>G ENSP00000353393.4:p.His1841Asp
NM_000132.3:c.5521C>G NP_000123.1:p.His1841Asp
XM_011531126.1:c.5416C>G XP_011529428.1:p.His1806Asp
NM_000132.4:c.5521C>G MANE Select NP_000123.1:p.His1841Asp
Search 100 bp 5'
Search 100 bp 3'