Canonical Allele Identifier: CA414901694
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154159626C>G (hg19) chrX:g.154931351C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931351C>G , CM000685.2:g.154931351C>G GRCh38
NC_000023.10:g.154159626C>G , CM000685.1:g.154159626C>G GRCh37
NC_000023.9:g.153812820C>G NCBI36
NG_011403.1:g.96373G>C
NG_011403.2:g.96373G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2439G>C MANE Select ENSP00000353393.4:p.Leu813Phe
ENST00000647125.1:c.*2105G>C ENSP00000496062.1:n.*2105G>C
ENST00000360256.8:c.2439G>C ENSP00000353393.4:p.Leu813Phe
NM_000132.3:c.2439G>C NP_000123.1:p.Leu813Phe
XM_011531126.1:c.2334G>C XP_011529428.1:p.Leu778Phe
NM_000132.4:c.2439G>C MANE Select NP_000123.1:p.Leu813Phe
Search 100 bp 5'
Search 100 bp 3'