Canonical Allele Identifier: CA2478924446
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1571464873

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884432C>T , CM000663.2:g.149884432C>T GRCh38
NC_000001.10:g.149855982C>T , CM000663.1:g.149855982C>T GRCh37
NC_000001.9:g.148122606C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1832G>A ENSP00000375736.2:n.377+1832G>A