Canonical Allele Identifier: CA414909181
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154905022-A-G
MyVariant Identifiers: chrX:g.154133297A>G (hg19) chrX:g.154905022A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905022A>G , CM000685.2:g.154905022A>G GRCh38
NC_000023.10:g.154133297A>G , CM000685.1:g.154133297A>G GRCh37
NC_000023.9:g.153786491A>G NCBI36
NG_011403.1:g.122702T>C
NG_011403.2:g.122702T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5375T>C MANE Select ENSP00000353393.4:p.Val1792Ala
ENST00000360256.8:c.5375T>C ENSP00000353393.4:p.Val1792Ala
NM_000132.3:c.5375T>C NP_000123.1:p.Val1792Ala
XM_011531126.1:c.5270T>C XP_011529428.1:p.Val1757Ala
NM_000132.4:c.5375T>C MANE Select NP_000123.1:p.Val1792Ala
Search 100 bp 5'
Search 100 bp 3'