Linked Data
gnomAD v4:
11-86954737-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.86954737C>T , CM000673.2:g.86954737C>T | GRCh38 |
| NC_000011.9:g.86665779C>T , CM000673.1:g.86665779C>T | GRCh37 |
| NC_000011.8:g.86343427C>T | NCBI36 |
| NG_011752.1:g.5655G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000531380.2:c.285+64G>A MANE Select | ENSP00000434034.1:n.285+64G>A | |
| ENST00000531380.1:c.285+64G>A | ENSP00000434034.1:n.285+64G>A | |
| NM_012193.3:c.285+64G>A | NP_036325.2:n.285+64G>A | |
| NM_012193.4:c.285+64G>A MANE Select | NP_036325.2:n.285+64G>A |