Linked Data
gnomAD v4:
12-52520337-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520337T>G , CM000674.2:g.52520337T>G | GRCh38 |
| NC_000012.11:g.52914121T>G , CM000674.1:g.52914121T>G | GRCh37 |
| NC_000012.10:g.51200388T>G | NCBI36 |
| NG_008297.1:g.5123A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.-41A>C MANE Select | ENSP00000252242.4:n.-41A>C | |
| ENST00000252242.8:c.-41A>C | ENSP00000252242.4:n.-41A>C | |
| ENST00000546577.1:c.-12-29A>C | ENSP00000449651.1:n.-12-29A>C | |
| ENST00000549420.1:c.-41A>C | ENSP00000447209.1:n.-41A>C | |
| ENST00000551275.1:c.-41A>C | ENSP00000448041.1:n.-41A>C | |
| ENST00000552629.5:n.58A>C | ||
| NM_000424.3:c.-41A>C | NP_000415.2:n.-41A>C | |
| NM_000424.4:c.-41A>C MANE Select | NP_000415.2:n.-41A>C |