Linked Data
gnomAD v4:
12-52520098-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520098T>C , CM000674.2:g.52520098T>C | GRCh38 |
| NC_000012.11:g.52913882T>C , CM000674.1:g.52913882T>C | GRCh37 |
| NC_000012.10:g.51200149T>C | NCBI36 |
| NG_008297.1:g.5362A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.199A>G MANE Select | ENSP00000252242.4:p.Asn67Asp | |
| ENST00000252242.8:c.199A>G | ENSP00000252242.4:p.Asn67Asp | |
| ENST00000546577.1:c.199A>G | ENSP00000449651.1:p.Asn67Asp | |
| ENST00000549420.1:c.43+156A>G | ENSP00000447209.1:n.43+156A>G | |
| ENST00000551275.1:c.172+27A>G | ENSP00000448041.1:n.172+27A>G | |
| ENST00000552629.5:n.297A>G | ||
| NM_000424.3:c.199A>G | NP_000415.2:p.Asn67Asp | |
| NM_000424.4:c.199A>G MANE Select | NP_000415.2:p.Asn67Asp |