Canonical Allele Identifier: CA425762390
Gene: RPL21P36 HGNC NCBI

Linked Data

gnomAD v4: 2-36299391-T-C
MyVariant Identifiers: chr2:g.36526534T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.36299391T>C , CM000664.2:g.36299391T>C GRCh38
NC_000002.11:g.36526534T>C , CM000664.1:g.36526534T>C GRCh37
NC_000002.10:g.36380038T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000427200.1:n.440A>G