Linked Data
gnomAD v4:
2-218893192-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218893192G>A , CM000664.2:g.218893192G>A | GRCh38 |
| NC_000002.11:g.219757914G>A , CM000664.1:g.219757914G>A | GRCh37 |
| NC_000002.10:g.219466158G>A | NCBI36 |
| NG_012179.1:g.17660G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.1175G>A MANE Select | ENSP00000258411.3:p.Cys392Tyr | |
| ENST00000258411.7:c.1175G>A | ENSP00000258411.3:p.Cys392Tyr | |
| NM_025216.2:c.1175G>A | NP_079492.2:p.Cys392Tyr | |
| XM_011511928.1:c.1124G>A | XP_011510230.1:p.Cys375Tyr | |
| XM_011511929.1:c.1079G>A | XP_011510231.1:p.Cys360Tyr | |
| XM_011511930.1:c.795G>A | XP_011510232.1:p.Leu265= | |
| XM_011511929.2:c.1079G>A | XP_011510231.1:p.Cys360Tyr | |
| NM_025216.3:c.1175G>A MANE Select | NP_079492.2:p.Cys392Tyr |