Canonical Allele Identifier: CA425762388
Gene: RPL21P36 HGNC NCBI

Linked Data

gnomAD v4: 2-36299390-A-T
MyVariant Identifiers: chr2:g.36526533A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.36299390A>T , CM000664.2:g.36299390A>T GRCh38
NC_000002.11:g.36526533A>T , CM000664.1:g.36526533A>T GRCh37
NC_000002.10:g.36380037A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000427200.1:n.441T>A