Canonical Allele Identifier: CA29966506
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs969244460
MyVariant Identifiers: chr1:g.149885223G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149885223G>A , CM000663.2:g.149885223G>A GRCh38
NC_000001.10:g.149856773G>A , CM000663.1:g.149856773G>A GRCh37
NC_000001.9:g.148123397G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1037C>T MANE Select ENSP00000358151.2:n.*1037C>T
ENST00000369155.3:c.*1037C>T ENSP00000358151.2:n.*1037C>T
ENST00000369160.3:c.377+1041C>T ENSP00000375736.2:n.377+1041C>T
NM_003528.2:c.*1037C>T NP_003519.1:n.*1037C>T
NM_003528.3:c.*1037C>T MANE Select NP_003519.1:n.*1037C>T
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