Linked Data
gnomAD v4:
5-140333197-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140333197A>G , CM000667.2:g.140333197A>G | GRCh38 |
| NC_000005.9:g.139712782A>G , CM000667.1:g.139712782A>G | GRCh37 |
| NC_000005.8:g.139692966A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230990.7:c.*1102T>C MANE Select | ENSP00000230990.6:n.*1102T>C | |
| ENST00000230990.6:c.*1102T>C | ENSP00000230990.6:n.*1102T>C | |
| NM_001945.2:c.*1102T>C | NP_001936.1:n.*1102T>C | |
| NM_001945.3:c.*1102T>C MANE Select | NP_001936.1:n.*1102T>C |