Canonical Allele Identifier: CA2568663430
Gene: H2BC21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884504C>G , CM000663.2:g.149884504C>G GRCh38
NC_000001.10:g.149856054C>G , CM000663.1:g.149856054C>G GRCh37
NC_000001.9:g.148122678C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1756G>C MANE Select ENSP00000358151.2:n.*1756G>C
ENST00000369155.3:c.*1756G>C ENSP00000358151.2:n.*1756G>C
ENST00000369160.3:c.377+1760G>C ENSP00000375736.2:n.377+1760G>C
NM_003528.2:c.*1756G>C NP_003519.1:n.*1756G>C
NM_003528.3:c.*1756G>C MANE Select NP_003519.1:n.*1756G>C
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