Canonical Allele Identifier: CA414917287
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154194944A>T (hg19) chrX:g.154966669A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966669A>T , CM000685.2:g.154966669A>T GRCh38
NC_000023.10:g.154194944A>T , CM000685.1:g.154194944A>T GRCh37
NC_000023.9:g.153848138A>T NCBI36
NG_011403.1:g.61055T>A
NG_011403.2:g.61055T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1028T>A MANE Select ENSP00000353393.4:p.Val343Asp
ENST00000647125.1:c.*904T>A ENSP00000496062.1:n.*904T>A
ENST00000360256.8:c.1028T>A ENSP00000353393.4:p.Val343Asp
NM_000132.3:c.1028T>A NP_000123.1:p.Val343Asp
XM_011531126.1:c.923T>A XP_011529428.1:p.Val308Asp
NM_000132.4:c.1028T>A MANE Select NP_000123.1:p.Val343Asp
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