Canonical Allele Identifier: CA5553438
Gene: MRPS16 HGNC NCBI
DNAJC9-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs374090427
ExAC: 10:75011777 A / C
gnomAD v2: 10-75011777-A-C
gnomAD v4: 10-73252019-A-C
MyVariant Identifiers: chr10:g.75011777A>C (hg19) chr10:g.73252019A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73252019A>C , CM000672.2:g.73252019A>C GRCh38
NC_000010.10:g.75011777A>C , CM000672.1:g.75011777A>C GRCh37
NC_000010.9:g.74681783A>C NCBI36
NG_008096.1:g.5675T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372945.8:c.18T>G (MRPS16) MANE Select ENSP00000362036.3:p.Thr6=
ENST00000372940.3:c.18T>G (MRPS16) ENSP00000362031.3:p.Thr6=
ENST00000372945.7:c.18T>G (MRPS16) ENSP00000362036.3:p.Thr6=
ENST00000471251.5:n.151T>G (MRPS16)
ENST00000473427.1:n.108T>G (MRPS16)
ENST00000479005.1:n.175T>G (MRPS16)
NM_016065.3:c.18T>G (MRPS16) NP_057149.1:p.Thr6=
NR_038373.1:n.175+3569A>C (DNAJC9-AS1)
XR_946059.1:n.120+278A>C
NM_016065.4:c.18T>G (MRPS16) MANE Select NP_057149.1:p.Thr6=
Search 100 bp 5'
Search 100 bp 3'