Canonical Allele Identifier: CA29966170
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs79555758
gnomAD v2: 1-149855904-C-T
gnomAD v3: 1-149884354-C-T
gnomAD v4: 1-149884354-C-T
MyVariant Identifiers: chr1:g.149855904C>T (hg19) chr1:g.149884354C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884354C>T , CM000663.2:g.149884354C>T GRCh38
NC_000001.10:g.149855904C>T , CM000663.1:g.149855904C>T GRCh37
NC_000001.9:g.148122528C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1910G>A ENSP00000375736.2:n.377+1910G>A
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