Linked Data
gnomAD v4:
3-150972831-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.150972831G>T , CM000665.2:g.150972831G>T | GRCh38 |
| NC_000003.11:g.150690618G>T , CM000665.1:g.150690618G>T | GRCh37 |
| NC_000003.10:g.152173308G>T | NCBI36 |
| NG_009168.1:g.5169C>A , LRG_700:g.5169C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327047.5:c.-123C>A (CLRN1) | ENSP00000322280.1:n.-123C>A | |
| NM_001195794.1:c.-123C>A , LRG_700t1:c.-123C>A (CLRN1) | NP_001182723.1:n.-123C>A | |
| NM_001256819.1:c.-123C>A (CLRN1) | NP_001243748.1:n.-123C>A | |
| NM_174878.2:c.-123C>A (CLRN1) | NP_777367.1:n.-123C>A | |
| NR_024066.1:n.154G>T (CLRN1-AS1) | ||
| NR_046380.2:n.169C>A (CLRN1) | ||
| XR_924167.1:n.190C>A (CLRN1) | ||
| NR_024066.2:n.154G>T (CLRN1-AS1) |