Canonical Allele Identifier: CA519384166
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225357A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997082A>T , CM000685.2:g.154997082A>T GRCh38
NC_000023.10:g.154225357A>T , CM000685.1:g.154225357A>T GRCh37
NC_000023.9:g.153878551A>T NCBI36
NG_011403.1:g.30642T>A
NG_011403.2:g.30642T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.279T>A MANE Select ENSP00000353393.4:p.Pro93=
ENST00000647125.1:c.*65T>A ENSP00000496062.1:n.*65T>A
ENST00000360256.8:c.279T>A ENSP00000353393.4:p.Pro93=
ENST00000423959.5:c.174T>A ENSP00000409446.1:p.Pro58=
ENST00000453950.1:c.261T>A ENSP00000389153.1:p.Pro87=
NM_000132.3:c.279T>A NP_000123.1:p.Pro93=
XM_011531126.1:c.174T>A XP_011529428.1:p.Pro58=
NM_000132.4:c.279T>A MANE Select NP_000123.1:p.Pro93=
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