Linked Data
gnomAD v4:
19-6713177-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713177A>G , CM000681.2:g.6713177A>G | GRCh38 |
| NC_000019.9:g.6713188A>G , CM000681.1:g.6713188A>G | GRCh37 |
| NC_000019.8:g.6664188A>G | NCBI36 |
| NG_009557.1:g.12475T>C , LRG_27:g.12475T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.880+12T>C | ENSP00000512083.1:n.880+12T>C | |
| ENST00000695654.1:c.127+12T>C | ENSP00000512085.1:n.127+12T>C | |
| ENST00000695692.1:n.327+12T>C | ||
| ENST00000245907.11:c.1003+12T>C MANE Select | ENSP00000245907.4:n.1003+12T>C | |
| ENST00000245907.10:c.1003+12T>C | ENSP00000245907.4:n.1003+12T>C | |
| ENST00000594270.5:n.127+12T>C | ||
| ENST00000595577.1:n.507+12T>C | ||
| ENST00000597442.5:n.253+12T>C | ||
| NM_000064.3:c.1003+12T>C | NP_000055.2:n.1003+12T>C | |
| NM_000064.4:c.1003+12T>C MANE Select | NP_000055.2:n.1003+12T>C |