Canonical Allele Identifier: CA2695167990
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154904056-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904057del , CM000685.2:g.154904057del GRCh38
NC_000023.10:g.154132332del , CM000685.1:g.154132332del GRCh37
NC_000023.9:g.153785526del NCBI36
NG_011403.1:g.123667del
NG_011403.2:g.123667del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5847del MANE Select ENSP00000353393.4:p.Gly1950AlafsTer2
ENST00000360256.8:c.5847del ENSP00000353393.4:p.Gly1950AlafsTer2
NM_000132.3:c.5847del NP_000123.1:p.Gly1950AlafsTer2
XM_011531126.1:c.5742del XP_011529428.1:p.Gly1915AlafsTer2
NM_000132.4:c.5847del MANE Select NP_000123.1:p.Gly1950AlafsTer2
Search 100 bp 5'
Search 100 bp 3'