Canonical Allele Identifier: CA16013831
Gene: F8 HGNC NCBI
dbSNP:
17281398
gnomAD v2:
X:154233774 A / G
gnomAD v3:
X:155005499 A / G
gnomAD v4:
chrX-155005499-A-G
Joint Max Group AF 0.09838339 (NFE)
Genomes Max Group AF 0.09838339 (NFE)
MyVariant.info:
GRCh38 chrX:g.155005499A>G
GRCh37 chrX:g.154233774A>G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155005499A>G , CM000685.2:g.155005499A>G GRCh38
NC_000023.10:g.154233774A>G , CM000685.1:g.154233774A>G GRCh37
NC_000023.9:g.153886968A>G NCBI36
NG_011403.1:g.22225T>C
NG_011403.2:g.22225T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.144-5899T>C MANE Select ENSP00000353393.4:n.144-5899T>C
ENST00000647125.1:c.122-5899T>C ENSP00000496062.1:n.122-5899T>C
ENST00000360256.8:c.144-5899T>C ENSP00000353393.4:n.144-5899T>C
ENST00000423959.5:c.39-5899T>C ENSP00000409446.1:n.39-5899T>C
ENST00000453950.1:c.126-5899T>C ENSP00000389153.1:n.126-5899T>C
NM_000132.3:c.144-5899T>C NP_000123.1:n.144-5899T>C
XM_011531126.1:c.39-5899T>C XP_011529428.1:n.39-5899T>C
NM_000132.4:c.144-5899T>C MANE Select NP_000123.1:n.144-5899T>C
Search 100 bp 5'
Search 100 bp 3'