Canonical Allele Identifier: CA889168442

Gene: H2BC21

Linked Data

• dbSNP Id: rs1343744429
• MyVariant Identifiers: chr1:g.149884346del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884346del , CM000663.2:g.149884346del	GRCh38
NC_000001.10:g.149855896del , CM000663.1:g.149855896del	GRCh37
NC_000001.9:g.148122520del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369160.3:c.377+1918del	ENSP00000375736.2:n.377+1918del