Canonical Allele Identifier: CA2647749609
Gene: H2BC21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884709A>G , CM000663.2:g.149884709A>G GRCh38
NC_000001.10:g.149856259A>G , CM000663.1:g.149856259A>G GRCh37
NC_000001.9:g.148122883A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1551T>C MANE Select ENSP00000358151.2:n.*1551T>C
ENST00000369155.3:c.*1551T>C ENSP00000358151.2:n.*1551T>C
ENST00000369160.3:c.377+1555T>C ENSP00000375736.2:n.377+1555T>C
NM_003528.2:c.*1551T>C NP_003519.1:n.*1551T>C
NM_003528.3:c.*1551T>C MANE Select NP_003519.1:n.*1551T>C