Linked Data
gnomAD v4:
2-85546545-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.85546545C>A , CM000664.2:g.85546545C>A | GRCh38 |
| NC_000002.11:g.85773668C>A , CM000664.1:g.85773668C>A | GRCh37 |
| NC_000002.10:g.85627179C>A | NCBI36 |
| NG_011811.2:g.19990G>T | |
| NG_029183.1:g.12568C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233838.9:c.*3389G>T MANE Select | ENSP00000233838.3:n.*3389G>T | |
| ENST00000233838.8:c.*3389G>T | ENSP00000233838.3:n.*3389G>T | |
| NM_000821.5:c.*3389G>T | NP_000812.2:n.*3389G>T | |
| NM_000821.6:c.*3389G>T | NP_000812.2:n.*3389G>T | |
| NM_001142269.2:c.*3389G>T | NP_001135741.1:n.*3389G>T | |
| NM_001142269.3:c.*3389G>T | NP_001135741.1:n.*3389G>T | |
| NM_000821.7:c.*3389G>T MANE Select | NP_000812.2:n.*3389G>T | |
| NM_001142269.4:c.*3389G>T | NP_001135741.1:n.*3389G>T |