Linked Data
gnomAD v4:
9-136687408-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136687408C>G , CM000671.2:g.136687408C>G | GRCh38 |
| NC_000009.11:g.139581860C>G , CM000671.1:g.139581860C>G | GRCh37 |
| NC_000009.10:g.138701681C>G | NCBI36 |
| NG_008090.1:g.5052G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.-51G>C MANE Select | ENSP00000360761.2:n.-51G>C | |
| ENST00000371696.6:c.-51G>C | ENSP00000360761.2:n.-51G>C | |
| NM_001012727.1:c.-51G>C | NP_001012745.1:n.-51G>C | |
| NM_006412.3:c.-51G>C | NP_006403.2:n.-51G>C | |
| NM_006412.4:c.-51G>C MANE Select | NP_006403.2:n.-51G>C | |
| NM_001012727.2:c.-51G>C | NP_001012745.1:n.-51G>C |