Canonical Allele Identifier: CA470285567
Gene: MRPS16 HGNC NCBI
DNAJC9-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs762611647
gnomAD v2: 10-75011639-G-T
gnomAD v4: 10-73251881-G-T
MyVariant Identifiers: chr10:g.75011639G>T (hg19) chr10:g.73251881G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73251881G>T , CM000672.2:g.73251881G>T GRCh38
NC_000010.10:g.75011639G>T , CM000672.1:g.75011639G>T GRCh37
NC_000010.9:g.74681645G>T NCBI36
NG_008096.1:g.5813C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372945.8:c.156C>A (MRPS16) MANE Select ENSP00000362036.3:p.Gly52=
ENST00000372940.3:c.156C>A (MRPS16) ENSP00000362031.3:p.Gly52=
ENST00000372945.7:c.156C>A (MRPS16) ENSP00000362036.3:p.Gly52=
ENST00000471251.5:n.289C>A (MRPS16)
ENST00000473427.1:n.246C>A (MRPS16)
ENST00000479005.1:n.313C>A (MRPS16)
NM_016065.3:c.156C>A (MRPS16) NP_057149.1:p.Gly52=
NR_038373.1:n.175+3431G>T (DNAJC9-AS1)
XR_946059.1:n.120+140G>T
NM_016065.4:c.156C>A (MRPS16) MANE Select NP_057149.1:p.Gly52=
Search 100 bp 5'
Search 100 bp 3'