Canonical Allele Identifier: CA414913929
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156963T>G (hg19) chrX:g.154928688T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928688T>G , CM000685.2:g.154928688T>G GRCh38
NC_000023.10:g.154156963T>G , CM000685.1:g.154156963T>G GRCh37
NC_000023.9:g.153810157T>G NCBI36
NG_011403.1:g.99036A>C
NG_011403.2:g.99036A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5102A>C MANE Select ENSP00000353393.4:p.Glu1701Ala
ENST00000360256.8:c.5102A>C ENSP00000353393.4:p.Glu1701Ala
NM_000132.3:c.5102A>C NP_000123.1:p.Glu1701Ala
XM_011531126.1:c.4997A>C XP_011529428.1:p.Glu1666Ala
NM_000132.4:c.5102A>C MANE Select NP_000123.1:p.Glu1701Ala
Search 100 bp 5'
Search 100 bp 3'