Canonical Allele Identifier: CA414908722
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154904912-T-C
MyVariant Identifiers: chrX:g.154133187T>C (hg19) chrX:g.154904912T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904912T>C , CM000685.2:g.154904912T>C GRCh38
NC_000023.10:g.154133187T>C , CM000685.1:g.154133187T>C GRCh37
NC_000023.9:g.153786381T>C NCBI36
NG_011403.1:g.122812A>G
NG_011403.2:g.122812A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5485A>G MANE Select ENSP00000353393.4:p.Asn1829Asp
ENST00000360256.8:c.5485A>G ENSP00000353393.4:p.Asn1829Asp
NM_000132.3:c.5485A>G NP_000123.1:p.Asn1829Asp
XM_011531126.1:c.5380A>G XP_011529428.1:p.Asn1794Asp
NM_000132.4:c.5485A>G MANE Select NP_000123.1:p.Asn1829Asp
Search 100 bp 5'
Search 100 bp 3'