Canonical Allele Identifier: CA873354165
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1246560892
gnomAD v3: X-154957368-A-T
gnomAD v4: X-154957368-A-T
MyVariant Identifiers: chrX:g.154957368A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957368A>T , CM000685.2:g.154957368A>T GRCh38
NC_000023.10:g.154185643A>T , CM000685.1:g.154185643A>T GRCh37
NC_000023.9:g.153838837A>T NCBI36
NG_011403.1:g.70356T>A
NG_011403.2:g.70356T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1538-197T>A MANE Select ENSP00000353393.4:n.1538-197T>A
ENST00000647125.1:c.*1414-197T>A ENSP00000496062.1:n.*1414-197T>A
ENST00000360256.8:c.1538-197T>A ENSP00000353393.4:n.1538-197T>A
NM_000132.3:c.1538-197T>A NP_000123.1:n.1538-197T>A
XM_011531126.1:c.1433-197T>A XP_011529428.1:n.1433-197T>A
NM_000132.4:c.1538-197T>A MANE Select NP_000123.1:n.1538-197T>A
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