Canonical Allele Identifier: CA526023819

Gene: H2BC21

Linked Data

• dbSNP Id: rs1553759462
• gnomAD v2: 1-149856063-A-C
• gnomAD v3: 1-149884513-A-C
• gnomAD v4: 1-149884513-A-C
• MyVariant Identifiers: chr1:g.149856063A>C (hg19) ; chr1:g.149884513A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884513A>C , CM000663.2:g.149884513A>C	GRCh38
NC_000001.10:g.149856063A>C , CM000663.1:g.149856063A>C	GRCh37
NC_000001.9:g.148122687A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1747T>G MANE Select	ENSP00000358151.2:n.*1747T>G
ENST00000369155.3:c.*1747T>G	ENSP00000358151.2:n.*1747T>G
ENST00000369160.3:c.377+1751T>G	ENSP00000375736.2:n.377+1751T>G
NM_003528.2:c.*1747T>G	NP_003519.1:n.*1747T>G
NM_003528.3:c.*1747T>G MANE Select	NP_003519.1:n.*1747T>G