Canonical Allele Identifier: CA526023792
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1320878617
gnomAD v2: 1-149855902-C-A
gnomAD v3: 1-149884352-C-A
gnomAD v4: 1-149884352-C-A
MyVariant Identifiers: chr1:g.149855902C>A (hg19) chr1:g.149884352C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884352C>A , CM000663.2:g.149884352C>A GRCh38
NC_000001.10:g.149855902C>A , CM000663.1:g.149855902C>A GRCh37
NC_000001.9:g.148122526C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1912G>T ENSP00000375736.2:n.377+1912G>T
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