Canonical Allele Identifier: CA10568058
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782704485
ExAC: X:154157119 C / T
gnomAD v2: X-154157119-C-T
gnomAD v4: X-154928844-C-T
MyVariant Identifiers: chrX:g.154157119C>T (hg19) chrX:g.154928844C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928844C>T , CM000685.2:g.154928844C>T GRCh38
NC_000023.10:g.154157119C>T , CM000685.1:g.154157119C>T GRCh37
NC_000023.9:g.153810313C>T NCBI36
NG_011403.1:g.98880G>A
NG_011403.2:g.98880G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4946G>A MANE Select ENSP00000353393.4:p.Gly1649Asp
ENST00000360256.8:c.4946G>A ENSP00000353393.4:p.Gly1649Asp
NM_000132.3:c.4946G>A NP_000123.1:p.Gly1649Asp
XM_011531126.1:c.4841G>A XP_011529428.1:p.Gly1614Asp
NM_000132.4:c.4946G>A MANE Select NP_000123.1:p.Gly1649Asp
Search 100 bp 5'
Search 100 bp 3'