Canonical Allele Identifier: CA526023806

Gene: H2BC21

Linked Data

• dbSNP Id: rs1553759459
• gnomAD v2: 1-149855969-T-C
• MyVariant Identifiers: chr1:g.149855969T>C (hg19) ; chr1:g.149884419T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884419T>C , CM000663.2:g.149884419T>C	GRCh38
NC_000001.10:g.149855969T>C , CM000663.1:g.149855969T>C	GRCh37
NC_000001.9:g.148122593T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369160.3:c.377+1845A>G	ENSP00000375736.2:n.377+1845A>G