Linked Data
gnomAD v4:
2-72891690-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.72891690G>T , CM000664.2:g.72891690G>T | GRCh38 |
| NC_000002.11:g.73118819G>T , CM000664.1:g.73118819G>T | GRCh37 |
| NC_000002.10:g.72972327G>T | NCBI36 |
| NG_008234.1:g.9308G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000234454.6:c.*153G>T MANE Select | ENSP00000234454.5:n.*153G>T | |
| ENST00000234454.5:c.*153G>T | ENSP00000234454.5:n.*153G>T | |
| ENST00000498749.1:n.884G>T | ||
| NM_003124.4:c.*153G>T | NP_003115.1:n.*153G>T | |
| NM_003124.5:c.*153G>T MANE Select | NP_003115.1:n.*153G>T |