Linked Data
gnomAD v4:
7-150861301-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150861301T>C , CM000669.2:g.150861301T>C | GRCh38 |
| NC_000007.13:g.150558389T>C , CM000669.1:g.150558389T>C | GRCh37 |
| NC_000007.12:g.150189322T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360937.9:c.*92T>C MANE Select | ENSP00000354193.4:n.*92T>C | |
| ENST00000360937.8:c.*92T>C | ENSP00000354193.4:n.*92T>C | |
| ENST00000467291.5:c.*92T>C | ENSP00000418328.1:n.*92T>C | |
| ENST00000493429.5:c.*92T>C | ENSP00000418614.1:n.*92T>C | |
| XR_928169.1:n.295+15708A>G | ||
| XR_928170.1:n.425+7315A>G | ||
| XR_928171.1:n.297+15708A>G | ||
| XR_928169.2:n.301+15708A>G | ||
| XR_928171.2:n.301+15708A>G | ||
| NM_001091.4:c.*92T>C MANE Select | NP_001082.2:n.*92T>C | |
| NM_001272072.2:c.*92T>C | NP_001259001.1:n.*92T>C |