Canonical Allele Identifier: CA916306492
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1424115344
gnomAD v4: 1-149885056-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149885064del , CM000663.2:g.149885064del GRCh38
NC_000001.10:g.149856614del , CM000663.1:g.149856614del GRCh37
NC_000001.9:g.148123238del NCBI36

Transcript Alleles

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