Canonical Allele Identifier: CA414909235
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154176037A>T (hg19) chrX:g.154947762A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154947762A>T , CM000685.2:g.154947762A>T GRCh38
NC_000023.10:g.154176037A>T , CM000685.1:g.154176037A>T GRCh37
NC_000023.9:g.153829231A>T NCBI36
NG_011403.1:g.79962T>A
NG_011403.2:g.79962T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.2049T>A MANE Select ENSP00000353393.4:p.Tyr683Ter
ENST00000647125.1:c.*1779+6130T>A ENSP00000496062.1:n.*1779+6130T>A
ENST00000360256.8:c.2049T>A ENSP00000353393.4:p.Tyr683Ter
NM_000132.3:c.2049T>A NP_000123.1:p.Tyr683Ter
XM_011531126.1:c.1944T>A XP_011529428.1:p.Tyr648Ter
NM_000132.4:c.2049T>A MANE Select NP_000123.1:p.Tyr683Ter
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