Canonical Allele Identifier: CA414916732
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154194853T>G (hg19) chrX:g.154966578T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966578T>G , CM000685.2:g.154966578T>G GRCh38
NC_000023.10:g.154194853T>G , CM000685.1:g.154194853T>G GRCh37
NC_000023.9:g.153848047T>G NCBI36
NG_011403.1:g.61146A>C
NG_011403.2:g.61146A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1119A>C MANE Select ENSP00000353393.4:p.Glu373Asp
ENST00000647125.1:c.*995A>C ENSP00000496062.1:n.*995A>C
ENST00000360256.8:c.1119A>C ENSP00000353393.4:p.Glu373Asp
NM_000132.3:c.1119A>C NP_000123.1:p.Glu373Asp
XM_011531126.1:c.1014A>C XP_011529428.1:p.Glu338Asp
NM_000132.4:c.1119A>C MANE Select NP_000123.1:p.Glu373Asp
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