Canonical Allele Identifier: CA1007547170

Gene: H2BC21

Linked Data

• dbSNP Id: rs2092284701
• gnomAD v3: 1-149884388-C-T
• gnomAD v4: 1-149884388-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884388C>T , CM000663.2:g.149884388C>T	GRCh38
NC_000001.10:g.149855938C>T , CM000663.1:g.149855938C>T	GRCh37
NC_000001.9:g.148122562C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369160.3:c.377+1876G>A	ENSP00000375736.2:n.377+1876G>A