Canonical Allele Identifier: CA439361429

Gene: RPL22P13

Linked Data

• MyVariant Identifiers: chr4:g.55087503T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54221336T>C , CM000666.2:g.54221336T>C	GRCh38
NC_000004.11:g.55087503T>C , CM000666.1:g.55087503T>C	GRCh37
NC_000004.10:g.54782260T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493291.1:n.211T>C
ENST00000507166.5:c.1018-53589T>C	ENSP00000423325.1:n.1018-53589T>C