Canonical Allele Identifier: CA2478924745
Gene: H2BC21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149885210C= , CM000663.2:g.149885210C= GRCh38
NC_000001.10:g.149856760C= , CM000663.1:g.149856760C= GRCh37
NC_000001.9:g.148123384C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1050G= MANE Select ENSP00000358151.2:n.*1050G=
ENST00000369155.3:c.*1050G= ENSP00000358151.2:n.*1050G=
ENST00000369160.3:c.377+1054G= ENSP00000375736.2:n.377+1054G=
NM_003528.2:c.*1050G= NP_003519.1:n.*1050G=
NM_003528.3:c.*1050G= MANE Select NP_003519.1:n.*1050G=
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