Canonical Allele Identifier: CA889168839
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1325668244
gnomAD v3: 1-149885193-TCATC-T
gnomAD v4: 1-149885193-TCATC-T
MyVariant Identifiers: chr1:g.149885194_149885197del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149885200_149885203del , CM000663.2:g.149885200_149885203del GRCh38
NC_000001.10:g.149856750_149856753del , CM000663.1:g.149856750_149856753del GRCh37
NC_000001.9:g.148123374_148123377del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1063_*1066del MANE Select ENSP00000358151.2:n.*1063_*1066del
ENST00000369155.3:c.*1063_*1066del ENSP00000358151.2:n.*1063_*1066del
ENST00000369160.3:c.377+1067_377+1070del ENSP00000375736.2:n.377+1067_377+1070del
NM_003528.2:c.*1063_*1066del NP_003519.1:n.*1063_*1066del
NM_003528.3:c.*1063_*1066del MANE Select NP_003519.1:n.*1063_*1066del
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