Canonical Allele Identifier: CA414914594
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154928806-A-C
MyVariant Identifiers: chrX:g.154157081A>C (hg19) chrX:g.154928806A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928806A>C , CM000685.2:g.154928806A>C GRCh38
NC_000023.10:g.154157081A>C , CM000685.1:g.154157081A>C GRCh37
NC_000023.9:g.153810275A>C NCBI36
NG_011403.1:g.98918T>G
NG_011403.2:g.98918T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4984T>G MANE Select ENSP00000353393.4:p.Leu1662Val
ENST00000360256.8:c.4984T>G ENSP00000353393.4:p.Leu1662Val
NM_000132.3:c.4984T>G NP_000123.1:p.Leu1662Val
XM_011531126.1:c.4879T>G XP_011529428.1:p.Leu1627Val
NM_000132.4:c.4984T>G MANE Select NP_000123.1:p.Leu1662Val
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