Canonical Allele Identifier: CA2695170426
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-155022292-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022292T>G , CM000685.2:g.155022292T>G GRCh38
NC_000023.10:g.154250567T>G , CM000685.1:g.154250567T>G GRCh37
NC_000023.9:g.153903761T>G NCBI36
NG_011403.1:g.5432A>C
NG_011403.2:g.5432A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.143+118A>C MANE Select ENSP00000353393.4:n.143+118A>C
ENST00000647125.1:c.121+140A>C ENSP00000496062.1:n.121+140A>C
ENST00000360256.8:c.143+118A>C ENSP00000353393.4:n.143+118A>C
ENST00000423959.5:c.38+4488A>C ENSP00000409446.1:n.38+4488A>C
ENST00000453950.1:c.125+118A>C ENSP00000389153.1:n.125+118A>C
NM_000132.3:c.143+118A>C NP_000123.1:n.143+118A>C
XM_011531126.1:c.38+4488A>C XP_011529428.1:n.38+4488A>C
NM_000132.4:c.143+118A>C MANE Select NP_000123.1:n.143+118A>C
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