Canonical Allele Identifier: CA889168447

Gene: H2BC21

Linked Data

• dbSNP Id: rs1445906303
• MyVariant Identifiers: chr1:g.149884381A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884381A>G , CM000663.2:g.149884381A>G	GRCh38
NC_000001.10:g.149855931A>G , CM000663.1:g.149855931A>G	GRCh37
NC_000001.9:g.148122555A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369160.3:c.377+1883T>C	ENSP00000375736.2:n.377+1883T>C