Canonical Allele Identifier: CA414914922
Gene: F8 HGNC NCBI

Linked Data

COSMIC: COSM1466919 COSM1466920
MyVariant Identifiers: chrX:g.154157126T>C (hg19) chrX:g.154928851T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928851T>C , CM000685.2:g.154928851T>C GRCh38
NC_000023.10:g.154157126T>C , CM000685.1:g.154157126T>C GRCh37
NC_000023.9:g.153810320T>C NCBI36
NG_011403.1:g.98873A>G
NG_011403.2:g.98873A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4939A>G MANE Select ENSP00000353393.4:p.Lys1647Glu
ENST00000360256.8:c.4939A>G ENSP00000353393.4:p.Lys1647Glu
NM_000132.3:c.4939A>G NP_000123.1:p.Lys1647Glu
XM_011531126.1:c.4834A>G XP_011529428.1:p.Lys1612Glu
NM_000132.4:c.4939A>G MANE Select NP_000123.1:p.Lys1647Glu
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