Canonical Allele Identifier: CA526023917
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1424115344
gnomAD v2: 1-149856606-C-CA
gnomAD v3: 1-149885056-C-CA
gnomAD v4: 1-149885056-C-CA
MyVariant Identifiers: chr1:g.149856606_149856607insA (hg19) chr1:g.149885056_149885057insA (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1203dup MANE Select ENSP00000358151.2:n.*1203dup
ENST00000369155.3:c.*1203dup ENSP00000358151.2:n.*1203dup
ENST00000369160.3:c.377+1207dup ENSP00000375736.2:n.377+1207dup
NM_003528.2:c.*1203dup NP_003519.1:n.*1203dup
NM_003528.3:c.*1203dup MANE Select NP_003519.1:n.*1203dup
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