Canonical Allele Identifier: CA414919983
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225302A>C (hg19) chrX:g.154997027A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997027A>C , CM000685.2:g.154997027A>C GRCh38
NC_000023.10:g.154225302A>C , CM000685.1:g.154225302A>C GRCh37
NC_000023.9:g.153878496A>C NCBI36
NG_011403.1:g.30697T>G
NG_011403.2:g.30697T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.334T>G MANE Select ENSP00000353393.4:p.Ser112Ala
ENST00000647125.1:c.*120T>G ENSP00000496062.1:n.*120T>G
ENST00000360256.8:c.334T>G ENSP00000353393.4:p.Ser112Ala
ENST00000423959.5:c.229T>G ENSP00000409446.1:p.Ser77Ala
ENST00000453950.1:c.316T>G ENSP00000389153.1:p.Ser106Ala
NM_000132.3:c.334T>G NP_000123.1:p.Ser112Ala
XM_011531126.1:c.229T>G XP_011529428.1:p.Ser77Ala
NM_000132.4:c.334T>G MANE Select NP_000123.1:p.Ser112Ala
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