Canonical Allele Identifier: CA414919385
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154221220A>G (hg19) chrX:g.154992945A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154992945A>G , CM000685.2:g.154992945A>G GRCh38
NC_000023.10:g.154221220A>G , CM000685.1:g.154221220A>G GRCh37
NC_000023.9:g.153874414A>G NCBI36
NG_011403.1:g.34779T>C
NG_011403.2:g.34779T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.592T>C MANE Select ENSP00000353393.4:p.Cys198Arg
ENST00000647125.1:c.*378T>C ENSP00000496062.1:n.*378T>C
ENST00000360256.8:c.592T>C ENSP00000353393.4:p.Cys198Arg
ENST00000423959.5:c.487T>C ENSP00000409446.1:p.Cys163Arg
NM_000132.3:c.592T>C NP_000123.1:p.Cys198Arg
XM_011531126.1:c.487T>C XP_011529428.1:p.Cys163Arg
NM_000132.4:c.592T>C MANE Select NP_000123.1:p.Cys198Arg
Search 100 bp 5'
Search 100 bp 3'