Canonical Allele Identifier: CA889168439
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1430471703
gnomAD v3: 1-149884344-T-C
gnomAD v4: 1-149884344-T-C
MyVariant Identifiers: chr1:g.149884344T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884344T>C , CM000663.2:g.149884344T>C GRCh38
NC_000001.10:g.149855894T>C , CM000663.1:g.149855894T>C GRCh37
NC_000001.9:g.148122518T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1920A>G ENSP00000375736.2:n.377+1920A>G
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