Canonical Allele Identifier: CA889168433
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1450518413
MyVariant Identifiers: chr1:g.149884338T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884338T>C , CM000663.2:g.149884338T>C GRCh38
NC_000001.10:g.149855888T>C , CM000663.1:g.149855888T>C GRCh37
NC_000001.9:g.148122512T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1926A>G ENSP00000375736.2:n.377+1926A>G
Search 100 bp 5'
Search 100 bp 3'