Canonical Allele Identifier: CA1007547461
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs2092289871
gnomAD v3: 1-149885219-A-G
gnomAD v4: 1-149885219-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149885219A>G , CM000663.2:g.149885219A>G GRCh38
NC_000001.10:g.149856769A>G , CM000663.1:g.149856769A>G GRCh37
NC_000001.9:g.148123393A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1041T>C MANE Select ENSP00000358151.2:n.*1041T>C
ENST00000369155.3:c.*1041T>C ENSP00000358151.2:n.*1041T>C
ENST00000369160.3:c.377+1045T>C ENSP00000375736.2:n.377+1045T>C
NM_003528.2:c.*1041T>C NP_003519.1:n.*1041T>C
NM_003528.3:c.*1041T>C MANE Select NP_003519.1:n.*1041T>C
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