Canonical Allele Identifier: CA414913695
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156910T>C (hg19) chrX:g.154928635T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928635T>C , CM000685.2:g.154928635T>C GRCh38
NC_000023.10:g.154156910T>C , CM000685.1:g.154156910T>C GRCh37
NC_000023.9:g.153810104T>C NCBI36
NG_011403.1:g.99089A>G
NG_011403.2:g.99089A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5155A>G MANE Select ENSP00000353393.4:p.Ile1719Val
ENST00000360256.8:c.5155A>G ENSP00000353393.4:p.Ile1719Val
NM_000132.3:c.5155A>G NP_000123.1:p.Ile1719Val
XM_011531126.1:c.5050A>G XP_011529428.1:p.Ile1684Val
NM_000132.4:c.5155A>G MANE Select NP_000123.1:p.Ile1719Val
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