Canonical Allele Identifier: CA414915952
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073424517
gnomAD v3: X-154966465-T-C
gnomAD v4: X-154966465-T-C
MyVariant Identifiers: chrX:g.154194740T>C (hg19) chrX:g.154966465T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966465T>C , CM000685.2:g.154966465T>C GRCh38
NC_000023.10:g.154194740T>C , CM000685.1:g.154194740T>C GRCh37
NC_000023.9:g.153847934T>C NCBI36
NG_011403.1:g.61259A>G
NG_011403.2:g.61259A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1232A>G MANE Select ENSP00000353393.4:p.Asp411Gly
ENST00000647125.1:c.*1108A>G ENSP00000496062.1:n.*1108A>G
ENST00000360256.8:c.1232A>G ENSP00000353393.4:p.Asp411Gly
ENST00000483822.2:n.52A>G
NM_000132.3:c.1232A>G NP_000123.1:p.Asp411Gly
XM_011531126.1:c.1127A>G XP_011529428.1:p.Asp376Gly
NM_000132.4:c.1232A>G MANE Select NP_000123.1:p.Asp411Gly
Search 100 bp 5'
Search 100 bp 3'