Canonical Allele Identifier: CA2602719877
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2123995767
gnomAD v3: X-154903700-T-A
gnomAD v4: X-154903700-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903700T>A , CM000685.2:g.154903700T>A GRCh38
NC_000023.10:g.154131975T>A , CM000685.1:g.154131975T>A GRCh37
NC_000023.9:g.153785169T>A NCBI36
NG_011403.1:g.124024A>T
NG_011403.2:g.124024A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5998+206A>T MANE Select ENSP00000353393.4:n.5998+206A>T
ENST00000360256.8:c.5998+206A>T ENSP00000353393.4:n.5998+206A>T
NM_000132.3:c.5998+206A>T NP_000123.1:n.5998+206A>T
XM_011531126.1:c.5893+206A>T XP_011529428.1:n.5893+206A>T
NM_000132.4:c.5998+206A>T MANE Select NP_000123.1:n.5998+206A>T
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