Canonical Allele Identifier: CA2478924595
Gene: H2BC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884825C= , CM000663.2:g.149884825C= GRCh38
NC_000001.10:g.149856375C= , CM000663.1:g.149856375C= GRCh37
NC_000001.9:g.148122999C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1435G= MANE Select ENSP00000358151.2:n.*1435G=
ENST00000369155.3:c.*1435G= ENSP00000358151.2:n.*1435G=
ENST00000369160.3:c.377+1439G= ENSP00000375736.2:n.377+1439G=
NM_003528.2:c.*1435G= NP_003519.1:n.*1435G=
NM_003528.3:c.*1435G= MANE Select NP_003519.1:n.*1435G=