Canonical Allele Identifier: CA45816157

Gene: RPL21P36

Linked Data

• dbSNP Id: rs887868803
• gnomAD v2: 2-36526532-T-C
• gnomAD v3: 2-36299389-T-C
• gnomAD v4: 2-36299389-T-C
• MyVariant Identifiers: chr2:g.36526532T>C (hg19) ; chr2:g.36299389T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.36299389T>C , CM000664.2:g.36299389T>C	GRCh38
NC_000002.11:g.36526532T>C , CM000664.1:g.36526532T>C	GRCh37
NC_000002.10:g.36380036T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427200.1:n.442A>G