Canonical Allele Identifier: CA414915480
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073175413
gnomAD v3: X-154928908-C-T
gnomAD v4: X-154928908-C-T
MyVariant Identifiers: chrX:g.154157183C>T (hg19) chrX:g.154928908C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928908C>T , CM000685.2:g.154928908C>T GRCh38
NC_000023.10:g.154157183C>T , CM000685.1:g.154157183C>T GRCh37
NC_000023.9:g.153810377C>T NCBI36
NG_011403.1:g.98816G>A
NG_011403.2:g.98816G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4882G>A MANE Select ENSP00000353393.4:p.Ala1628Thr
ENST00000360256.8:c.4882G>A ENSP00000353393.4:p.Ala1628Thr
NM_000132.3:c.4882G>A NP_000123.1:p.Ala1628Thr
XM_011531126.1:c.4777G>A XP_011529428.1:p.Ala1593Thr
NM_000132.4:c.4882G>A MANE Select NP_000123.1:p.Ala1628Thr
Search 100 bp 5'
Search 100 bp 3'