Canonical Allele Identifier: CA2647749622
Gene: H2BC21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884733G>A , CM000663.2:g.149884733G>A GRCh38
NC_000001.10:g.149856283G>A , CM000663.1:g.149856283G>A GRCh37
NC_000001.9:g.148122907G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1527C>T MANE Select ENSP00000358151.2:n.*1527C>T
ENST00000369155.3:c.*1527C>T ENSP00000358151.2:n.*1527C>T
ENST00000369160.3:c.377+1531C>T ENSP00000375736.2:n.377+1531C>T
NM_003528.2:c.*1527C>T NP_003519.1:n.*1527C>T
NM_003528.3:c.*1527C>T MANE Select NP_003519.1:n.*1527C>T