Canonical Allele Identifier: CA2695170451
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-155022322-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022322T>C , CM000685.2:g.155022322T>C GRCh38
NC_000023.10:g.154250597T>C , CM000685.1:g.154250597T>C GRCh37
NC_000023.9:g.153903791T>C NCBI36
NG_011403.1:g.5402A>G
NG_011403.2:g.5402A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.143+88A>G MANE Select ENSP00000353393.4:n.143+88A>G
ENST00000647125.1:c.121+110A>G ENSP00000496062.1:n.121+110A>G
ENST00000360256.8:c.143+88A>G ENSP00000353393.4:n.143+88A>G
ENST00000423959.5:c.38+4458A>G ENSP00000409446.1:n.38+4458A>G
ENST00000453950.1:c.125+88A>G ENSP00000389153.1:n.125+88A>G
NM_000132.3:c.143+88A>G NP_000123.1:n.143+88A>G
XM_011531126.1:c.38+4458A>G XP_011529428.1:n.38+4458A>G
NM_000132.4:c.143+88A>G MANE Select NP_000123.1:n.143+88A>G
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