Canonical Allele Identifier: CA2647749725
Gene: H2BC21 HGNC NCBI

Linked Data

gnomAD v4: 1-149885056-C-CATTAAAAAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149885057_149885058insTTAAAAAAA , CM000663.2:g.149885057_149885058insTTAAAAAAA GRCh38
NC_000001.10:g.149856607_149856608insTTAAAAAAA , CM000663.1:g.149856607_149856608insTTAAAAAAA GRCh37
NC_000001.9:g.148123231_148123232insTTAAAAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1203_*1204insTTTTTTAAT MANE Select ENSP00000358151.2:n.*1203_*1204insTTTTTTAAT
ENST00000369155.3:c.*1203_*1204insTTTTTTAAT ENSP00000358151.2:n.*1203_*1204insTTTTTTAAT
ENST00000369160.3:c.377+1207_377+1208insTTTTTTAAT ENSP00000375736.2:n.377+1207_377+1208insTTTTTTAAT
NM_003528.2:c.*1203_*1204insTTTTTTAAT NP_003519.1:n.*1203_*1204insTTTTTTAAT
NM_003528.3:c.*1203_*1204insTTTTTTAAT MANE Select NP_003519.1:n.*1203_*1204insTTTTTTAAT
Search 100 bp 5'
Search 100 bp 3'