Canonical Allele Identifier: CA2695152106
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154896333-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896333T>A , CM000685.2:g.154896333T>A GRCh38
NC_000023.10:g.154124608T>A , CM000685.1:g.154124608T>A GRCh37
NC_000023.9:g.153777802T>A NCBI36
NG_011403.1:g.131391A>T
NG_011403.2:g.131391A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6274-101A>T MANE Select ENSP00000353393.4:n.6274-101A>T
ENST00000360256.8:c.6274-101A>T ENSP00000353393.4:n.6274-101A>T
NM_000132.3:c.6274-101A>T NP_000123.1:n.6274-101A>T
XM_011531126.1:c.6169-101A>T XP_011529428.1:n.6169-101A>T
NM_000132.4:c.6274-101A>T MANE Select NP_000123.1:n.6274-101A>T
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