Canonical Allele Identifier: CA889168456
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1185504782
MyVariant Identifiers: chr1:g.149884405G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884405G>A , CM000663.2:g.149884405G>A GRCh38
NC_000001.10:g.149855955G>A , CM000663.1:g.149855955G>A GRCh37
NC_000001.9:g.148122579G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1859C>T ENSP00000375736.2:n.377+1859C>T
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