Canonical Allele Identifier: CA2478924594
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1571465221

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884822A>C , CM000663.2:g.149884822A>C GRCh38
NC_000001.10:g.149856372A>C , CM000663.1:g.149856372A>C GRCh37
NC_000001.9:g.148122996A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1438T>G MANE Select ENSP00000358151.2:n.*1438T>G
ENST00000369155.3:c.*1438T>G ENSP00000358151.2:n.*1438T>G
ENST00000369160.3:c.377+1442T>G ENSP00000375736.2:n.377+1442T>G
NM_003528.2:c.*1438T>G NP_003519.1:n.*1438T>G
NM_003528.3:c.*1438T>G MANE Select NP_003519.1:n.*1438T>G