Canonical Allele Identifier: CA1138596671
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073020619
gnomAD v3: X-154903518-A-AT
gnomAD v4: X-154903518-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903520dup , CM000685.2:g.154903520dup GRCh38
NC_000023.10:g.154131795dup , CM000685.1:g.154131795dup GRCh37
NC_000023.9:g.153784989dup NCBI36
NG_011403.1:g.124205dup
NG_011403.2:g.124205dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5998+387dup MANE Select ENSP00000353393.4:n.5998+387dup
ENST00000360256.8:c.5998+387dup ENSP00000353393.4:n.5998+387dup
NM_000132.3:c.5998+387dup NP_000123.1:n.5998+387dup
XM_011531126.1:c.5893+387dup XP_011529428.1:n.5893+387dup
NM_000132.4:c.5998+387dup MANE Select NP_000123.1:n.5998+387dup
Search 100 bp 5'
Search 100 bp 3'