Canonical Allele Identifier: CA519718971
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154928876-C-T
MyVariant Identifiers: chrX:g.154157151C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928876C>T , CM000685.2:g.154928876C>T GRCh38
NC_000023.10:g.154157151C>T , CM000685.1:g.154157151C>T GRCh37
NC_000023.9:g.153810345C>T NCBI36
NG_011403.1:g.98848G>A
NG_011403.2:g.98848G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4914G>A MANE Select ENSP00000353393.4:p.Lys1638=
ENST00000360256.8:c.4914G>A ENSP00000353393.4:p.Lys1638=
NM_000132.3:c.4914G>A NP_000123.1:p.Lys1638=
XM_011531126.1:c.4809G>A XP_011529428.1:p.Lys1603=
NM_000132.4:c.4914G>A MANE Select NP_000123.1:p.Lys1638=
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