Canonical Allele Identifier: CA2478924422
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs2092284727

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884389A>C , CM000663.2:g.149884389A>C GRCh38
NC_000001.10:g.149855939A>C , CM000663.1:g.149855939A>C GRCh37
NC_000001.9:g.148122563A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1875T>G ENSP00000375736.2:n.377+1875T>G