Canonical Allele Identifier: CA414919374
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154221215T>G (hg19) chrX:g.154992940T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154992940T>G , CM000685.2:g.154992940T>G GRCh38
NC_000023.10:g.154221215T>G , CM000685.1:g.154221215T>G GRCh37
NC_000023.9:g.153874409T>G NCBI36
NG_011403.1:g.34784A>C
NG_011403.2:g.34784A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.597A>C MANE Select ENSP00000353393.4:p.Arg199Ser
ENST00000647125.1:c.*383A>C ENSP00000496062.1:n.*383A>C
ENST00000360256.8:c.597A>C ENSP00000353393.4:p.Arg199Ser
ENST00000423959.5:c.492A>C ENSP00000409446.1:p.Arg164Ser
NM_000132.3:c.597A>C NP_000123.1:p.Arg199Ser
XM_011531126.1:c.492A>C XP_011529428.1:p.Arg164Ser
NM_000132.4:c.597A>C MANE Select NP_000123.1:p.Arg199Ser
Search 100 bp 5'
Search 100 bp 3'