Canonical Allele Identifier: CA10568051
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs781804567
ExAC: X:154157079 C / T
gnomAD v2: X-154157079-C-T
gnomAD v3: X-154928804-C-T
gnomAD v4: X-154928804-C-T
MyVariant Identifiers: chrX:g.154157079C>T (hg19) chrX:g.154928804C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928804C>T , CM000685.2:g.154928804C>T GRCh38
NC_000023.10:g.154157079C>T , CM000685.1:g.154157079C>T GRCh37
NC_000023.9:g.153810273C>T NCBI36
NG_011403.1:g.98920G>A
NG_011403.2:g.98920G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4986G>A MANE Select ENSP00000353393.4:p.Leu1662=
ENST00000360256.8:c.4986G>A ENSP00000353393.4:p.Leu1662=
NM_000132.3:c.4986G>A NP_000123.1:p.Leu1662=
XM_011531126.1:c.4881G>A XP_011529428.1:p.Leu1627=
NM_000132.4:c.4986G>A MANE Select NP_000123.1:p.Leu1662=
Search 100 bp 5'
Search 100 bp 3'