Canonical Allele Identifier: CA2647749658
Gene: H2BC21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884850C>A , CM000663.2:g.149884850C>A GRCh38
NC_000001.10:g.149856400C>A , CM000663.1:g.149856400C>A GRCh37
NC_000001.9:g.148123024C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1410G>T MANE Select ENSP00000358151.2:n.*1410G>T
ENST00000369155.3:c.*1410G>T ENSP00000358151.2:n.*1410G>T
ENST00000369160.3:c.377+1414G>T ENSP00000375736.2:n.377+1414G>T
NM_003528.2:c.*1410G>T NP_003519.1:n.*1410G>T
NM_003528.3:c.*1410G>T MANE Select NP_003519.1:n.*1410G>T