Canonical Allele Identifier: CA2478924426
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs2092284777

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884393G>C , CM000663.2:g.149884393G>C GRCh38
NC_000001.10:g.149855943G>C , CM000663.1:g.149855943G>C GRCh37
NC_000001.9:g.148122567G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1871C>G ENSP00000375736.2:n.377+1871C>G