Linked Data
gnomAD v4:
19-6714220-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714220A>C , CM000681.2:g.6714220A>C | GRCh38 |
| NC_000019.9:g.6714231A>C , CM000681.1:g.6714231A>C | GRCh37 |
| NC_000019.8:g.6665231A>C | NCBI36 |
| NG_009557.1:g.11432T>G , LRG_27:g.11432T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.505T>G | ENSP00000512083.1:p.Tyr169Asp | |
| ENST00000245907.11:c.628T>G MANE Select | ENSP00000245907.4:p.Tyr210Asp | |
| ENST00000245907.10:c.628T>G | ENSP00000245907.4:p.Tyr210Asp | |
| ENST00000595577.1:n.132T>G | ||
| NM_000064.3:c.628T>G | NP_000055.2:p.Tyr210Asp | |
| NM_000064.4:c.628T>G MANE Select | NP_000055.2:p.Tyr210Asp |