Canonical Allele Identifier: CA889168450
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1414155601
MyVariant Identifiers: chr1:g.149884401A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884401A>C , CM000663.2:g.149884401A>C GRCh38
NC_000001.10:g.149855951A>C , CM000663.1:g.149855951A>C GRCh37
NC_000001.9:g.148122575A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1863T>G ENSP00000375736.2:n.377+1863T>G
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