Canonical Allele Identifier: CA29966407
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs15931

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884800C>T , CM000663.2:g.149884800C>T GRCh38
NC_000001.10:g.149856350C>T , CM000663.1:g.149856350C>T GRCh37
NC_000001.9:g.148122974C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1460G>A MANE Select ENSP00000358151.2:n.*1460G>A
ENST00000369155.3:c.*1460G>A ENSP00000358151.2:n.*1460G>A
ENST00000369160.3:c.377+1464G>A ENSP00000375736.2:n.377+1464G>A
NM_003528.2:c.*1460G>A NP_003519.1:n.*1460G>A
NM_003528.3:c.*1460G>A MANE Select NP_003519.1:n.*1460G>A