Canonical Allele Identifier: CA889168657
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1417415659
gnomAD v3: 1-149884884-T-C
gnomAD v4: 1-149884884-T-C
MyVariant Identifiers: chr1:g.149884884T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884884T>C , CM000663.2:g.149884884T>C GRCh38
NC_000001.10:g.149856434T>C , CM000663.1:g.149856434T>C GRCh37
NC_000001.9:g.148123058T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1376A>G MANE Select ENSP00000358151.2:n.*1376A>G
ENST00000369155.3:c.*1376A>G ENSP00000358151.2:n.*1376A>G
ENST00000369160.3:c.377+1380A>G ENSP00000375736.2:n.377+1380A>G
NM_003528.2:c.*1376A>G NP_003519.1:n.*1376A>G
NM_003528.3:c.*1376A>G MANE Select NP_003519.1:n.*1376A>G
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