Canonical Allele Identifier: CA2478924617
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs2092287666

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884878T>A , CM000663.2:g.149884878T>A GRCh38
NC_000001.10:g.149856428T>A , CM000663.1:g.149856428T>A GRCh37
NC_000001.9:g.148123052T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1382A>T MANE Select ENSP00000358151.2:n.*1382A>T
ENST00000369155.3:c.*1382A>T ENSP00000358151.2:n.*1382A>T
ENST00000369160.3:c.377+1386A>T ENSP00000375736.2:n.377+1386A>T
NM_003528.2:c.*1382A>T NP_003519.1:n.*1382A>T
NM_003528.3:c.*1382A>T MANE Select NP_003519.1:n.*1382A>T