Canonical Allele Identifier: CA5553408
Gene: MRPS16 HGNC NCBI
DNAJC9-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs758576112
ExAC: 10:75011686 C / T
gnomAD v2: 10-75011686-C-T
gnomAD v4: 10-73251928-C-T
MyVariant Identifiers: chr10:g.75011686C>T (hg19) chr10:g.73251928C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73251928C>T , CM000672.2:g.73251928C>T GRCh38
NC_000010.10:g.75011686C>T , CM000672.1:g.75011686C>T GRCh37
NC_000010.9:g.74681692C>T NCBI36
NG_008096.1:g.5766G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372945.8:c.109G>A (MRPS16) MANE Select ENSP00000362036.3:p.Ala37Thr
ENST00000372940.3:c.109G>A (MRPS16) ENSP00000362031.3:p.Ala37Thr
ENST00000372945.7:c.109G>A (MRPS16) ENSP00000362036.3:p.Ala37Thr
ENST00000471251.5:n.242G>A (MRPS16)
ENST00000473427.1:n.199G>A (MRPS16)
ENST00000479005.1:n.266G>A (MRPS16)
NM_016065.3:c.109G>A (MRPS16) NP_057149.1:p.Ala37Thr
NR_038373.1:n.175+3478C>T (DNAJC9-AS1)
XR_946059.1:n.120+187C>T
NM_016065.4:c.109G>A (MRPS16) MANE Select NP_057149.1:p.Ala37Thr
Search 100 bp 5'
Search 100 bp 3'