Canonical Allele Identifier: CA889168525
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1203874546
gnomAD v3: 1-149884627-A-T
gnomAD v4: 1-149884627-A-T
MyVariant Identifiers: chr1:g.149884627A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884627A>T , CM000663.2:g.149884627A>T GRCh38
NC_000001.10:g.149856177A>T , CM000663.1:g.149856177A>T GRCh37
NC_000001.9:g.148122801A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1633T>A MANE Select ENSP00000358151.2:n.*1633T>A
ENST00000369155.3:c.*1633T>A ENSP00000358151.2:n.*1633T>A
ENST00000369160.3:c.377+1637T>A ENSP00000375736.2:n.377+1637T>A
NM_003528.2:c.*1633T>A NP_003519.1:n.*1633T>A
NM_003528.3:c.*1633T>A MANE Select NP_003519.1:n.*1633T>A
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