Canonical Allele Identifier: CA2647749648

Gene: H2BC21

Linked Data

• gnomAD v4: 1-149884831-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884831T>A , CM000663.2:g.149884831T>A	GRCh38
NC_000001.10:g.149856381T>A , CM000663.1:g.149856381T>A	GRCh37
NC_000001.9:g.148123005T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1429A>T MANE Select	ENSP00000358151.2:n.*1429A>T
ENST00000369155.3:c.*1429A>T	ENSP00000358151.2:n.*1429A>T
ENST00000369160.3:c.377+1433A>T	ENSP00000375736.2:n.377+1433A>T
NM_003528.2:c.*1429A>T	NP_003519.1:n.*1429A>T
NM_003528.3:c.*1429A>T MANE Select	NP_003519.1:n.*1429A>T