Canonical Allele Identifier: CA29966193

Gene: H2BC21

Linked Data

• dbSNP Id: rs983973521
• MyVariant Identifiers: chr1:g.149884368C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884368C>T , CM000663.2:g.149884368C>T	GRCh38
NC_000001.10:g.149855918C>T , CM000663.1:g.149855918C>T	GRCh37
NC_000001.9:g.148122542C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369160.3:c.377+1896G>A	ENSP00000375736.2:n.377+1896G>A