Canonical Allele Identifier: CA1007547182

Gene: H2BC21

Linked Data

• dbSNP Id: rs2092284990
• gnomAD v3: 1-149884433-T-C
• gnomAD v4: 1-149884433-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884433T>C , CM000663.2:g.149884433T>C	GRCh38
NC_000001.10:g.149855983T>C , CM000663.1:g.149855983T>C	GRCh37
NC_000001.9:g.148122607T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369160.3:c.377+1831A>G	ENSP00000375736.2:n.377+1831A>G