Linked Data
gnomAD v4:
7-152648928-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152648928T>G , CM000669.2:g.152648928T>G | GRCh38 |
| NC_000007.13:g.152346013T>G , CM000669.1:g.152346013T>G | GRCh37 |
| NC_000007.12:g.151976946T>G | NCBI36 |
| NG_027988.1:g.32238A>C | |
| NG_027988.2:g.32238A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698506.1:c.389A>C | ENSP00000513758.1:p.Asp130Ala | |
| ENST00000359321.2:c.557A>C MANE Select | ENSP00000352271.1:p.Asp186Ala | |
| ENST00000359321.1:c.557A>C | ENSP00000352271.1:p.Asp186Ala | |
| ENST00000495707.1:n.579A>C | ||
| NM_005431.1:c.557A>C | NP_005422.1:p.Asp186Ala | |
| NM_005431.2:c.557A>C MANE Select | NP_005422.1:p.Asp186Ala |