Canonical Allele Identifier: CA889168653
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1466349941
gnomAD v3: 1-149884873-G-A
gnomAD v4: 1-149884873-G-A
MyVariant Identifiers: chr1:g.149884873G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884873G>A , CM000663.2:g.149884873G>A GRCh38
NC_000001.10:g.149856423G>A , CM000663.1:g.149856423G>A GRCh37
NC_000001.9:g.148123047G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1387C>T MANE Select ENSP00000358151.2:n.*1387C>T
ENST00000369155.3:c.*1387C>T ENSP00000358151.2:n.*1387C>T
ENST00000369160.3:c.377+1391C>T ENSP00000375736.2:n.377+1391C>T
NM_003528.2:c.*1387C>T NP_003519.1:n.*1387C>T
NM_003528.3:c.*1387C>T MANE Select NP_003519.1:n.*1387C>T
Search 100 bp 5'
Search 100 bp 3'