Linked Data
gnomAD v4:
7-152649188-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152649188T>A , CM000669.2:g.152649188T>A | GRCh38 |
| NC_000007.13:g.152346273T>A , CM000669.1:g.152346273T>A | GRCh37 |
| NC_000007.12:g.151977206T>A | NCBI36 |
| NG_027988.1:g.31978A>T | |
| NG_027988.2:g.31978A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698506.1:c.129A>T | ENSP00000513758.1:p.Arg43Ser | |
| ENST00000359321.2:c.297A>T MANE Select | ENSP00000352271.1:p.Arg99Ser | |
| ENST00000359321.1:c.297A>T | ENSP00000352271.1:p.Arg99Ser | |
| ENST00000495707.1:n.319A>T | ||
| NM_005431.1:c.297A>T | NP_005422.1:p.Arg99Ser | |
| NM_005431.2:c.297A>T MANE Select | NP_005422.1:p.Arg99Ser |