Canonical Allele Identifier: CA414919643
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154221340G>C (hg19) chrX:g.154993065G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993065G>C , CM000685.2:g.154993065G>C GRCh38
NC_000023.10:g.154221340G>C , CM000685.1:g.154221340G>C GRCh37
NC_000023.9:g.153874534G>C NCBI36
NG_011403.1:g.34659C>G
NG_011403.2:g.34659C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.472C>G MANE Select ENSP00000353393.4:p.Gln158Glu
ENST00000647125.1:c.*258C>G ENSP00000496062.1:n.*258C>G
ENST00000360256.8:c.472C>G ENSP00000353393.4:p.Gln158Glu
ENST00000423959.5:c.367C>G ENSP00000409446.1:p.Gln123Glu
ENST00000453950.1:c.454C>G ENSP00000389153.1:p.Gln152Glu
NM_000132.3:c.472C>G NP_000123.1:p.Gln158Glu
XM_011531126.1:c.367C>G XP_011529428.1:p.Gln123Glu
NM_000132.4:c.472C>G MANE Select NP_000123.1:p.Gln158Glu
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