Canonical Allele Identifier: CA29966231

Gene: H2BC21

Linked Data

• dbSNP Id: rs782399070
• MyVariant Identifiers: chr1:g.149856005A>C (hg19) ; chr1:g.149884455A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884455A>C , CM000663.2:g.149884455A>C	GRCh38
NC_000001.10:g.149856005A>C , CM000663.1:g.149856005A>C	GRCh37
NC_000001.9:g.148122629A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369160.3:c.377+1809T>G	ENSP00000375736.2:n.377+1809T>G