Linked Data
gnomAD v4:
1-114707212-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114707212A>G , CM000663.2:g.114707212A>G | GRCh38 |
| NC_000001.10:g.115249833A>G , CM000663.1:g.115249833A>G | GRCh37 |
| NC_000001.9:g.115051356A>G | NCBI36 |
| NG_007572.1:g.14683T>C , LRG_92:g.14683T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.*882T>C MANE Select | ENSP00000358548.4:n.*882T>C | |
| ENST00000369535.4:c.*882T>C | ENSP00000358548.4:n.*882T>C | |
| NM_002524.4:c.*882T>C | NP_002515.1:n.*882T>C | |
| NM_002524.5:c.*882T>C MANE Select | NP_002515.1:n.*882T>C |