Canonical Allele Identifier: CA414901702
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154931355-A-G
MyVariant Identifiers: chrX:g.154159630A>G (hg19) chrX:g.154931355A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931355A>G , CM000685.2:g.154931355A>G GRCh38
NC_000023.10:g.154159630A>G , CM000685.1:g.154159630A>G GRCh37
NC_000023.9:g.153812824A>G NCBI36
NG_011403.1:g.96369T>C
NG_011403.2:g.96369T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.2435T>C MANE Select ENSP00000353393.4:p.Leu812Pro
ENST00000647125.1:c.*2101T>C ENSP00000496062.1:n.*2101T>C
ENST00000360256.8:c.2435T>C ENSP00000353393.4:p.Leu812Pro
NM_000132.3:c.2435T>C NP_000123.1:p.Leu812Pro
XM_011531126.1:c.2330T>C XP_011529428.1:p.Leu777Pro
NM_000132.4:c.2435T>C MANE Select NP_000123.1:p.Leu812Pro
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