Linked Data
gnomAD v4:
7-152660559-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152660559G>T , CM000669.2:g.152660559G>T | GRCh38 |
| NC_000007.13:g.152357644G>T , CM000669.1:g.152357644G>T | GRCh37 |
| NC_000007.12:g.151988577G>T | NCBI36 |
| NG_027988.1:g.20607C>A | |
| NG_027988.2:g.20607C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698506.1:c.-47-11196C>A | ENSP00000513758.1:n.-47-11196C>A | |
| ENST00000698507.1:n.331C>A | ||
| ENST00000359321.2:c.121+142C>A MANE Select | ENSP00000352271.1:n.121+142C>A | |
| ENST00000359321.1:c.121+142C>A | ENSP00000352271.1:n.121+142C>A | |
| ENST00000495707.1:n.143+142C>A | ||
| NM_005431.1:c.121+142C>A | NP_005422.1:n.121+142C>A | |
| NM_005431.2:c.121+142C>A MANE Select | NP_005422.1:n.121+142C>A |