Canonical Allele Identifier: CA414904460
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154130326T>G (hg19) chrX:g.154902051T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902051T>G , CM000685.2:g.154902051T>G GRCh38
NC_000023.10:g.154130326T>G , CM000685.1:g.154130326T>G GRCh37
NC_000023.9:g.153783520T>G NCBI36
NG_011403.1:g.125673A>C
NG_011403.2:g.125673A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6115A>C MANE Select ENSP00000353393.4:p.Lys2039Gln
ENST00000360256.8:c.6115A>C ENSP00000353393.4:p.Lys2039Gln
NM_000132.3:c.6115A>C NP_000123.1:p.Lys2039Gln
XM_011531126.1:c.6010A>C XP_011529428.1:p.Lys2004Gln
NM_000132.4:c.6115A>C MANE Select NP_000123.1:p.Lys2039Gln
Search 100 bp 5'
Search 100 bp 3'