Canonical Allele Identifier: CA889168650
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1466349941
gnomAD v3: 1-149884873-G-T
gnomAD v4: 1-149884873-G-T
MyVariant Identifiers: chr1:g.149884873G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884873G>T , CM000663.2:g.149884873G>T GRCh38
NC_000001.10:g.149856423G>T , CM000663.1:g.149856423G>T GRCh37
NC_000001.9:g.148123047G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1387C>A MANE Select ENSP00000358151.2:n.*1387C>A
ENST00000369155.3:c.*1387C>A ENSP00000358151.2:n.*1387C>A
ENST00000369160.3:c.377+1391C>A ENSP00000375736.2:n.377+1391C>A
NM_003528.2:c.*1387C>A NP_003519.1:n.*1387C>A
NM_003528.3:c.*1387C>A MANE Select NP_003519.1:n.*1387C>A
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