Canonical Allele Identifier: CA2478924427
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1571464843
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884397T>G , CM000663.2:g.149884397T>G GRCh38
NC_000001.10:g.149855947T>G , CM000663.1:g.149855947T>G GRCh37
NC_000001.9:g.148122571T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1867A>C ENSP00000375736.2:n.377+1867A>C
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