Linked Data
gnomAD v4:
19-55154473-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154473A>G , CM000681.2:g.55154473A>G | GRCh38 |
| NC_000019.9:g.55665841A>G , CM000681.1:g.55665841A>G | GRCh37 |
| NC_000019.8:g.60357653A>G | NCBI36 |
| NG_007866.2:g.8260T>C , LRG_432:g.8260T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.373-267T>C MANE Select | ENSP00000341838.5:n.373-267T>C | |
| ENST00000665070.1:c.405+235T>C | ENSP00000499482.1:n.405+235T>C | |
| ENST00000344887.9:c.373-267T>C | ENSP00000341838.5:n.373-267T>C | |
| ENST00000585806.5:n.372-267T>C | ||
| ENST00000586669.5:n.381-267T>C | ||
| ENST00000587176.5:n.824T>C | ||
| ENST00000588882.1:c.298-267T>C | ENSP00000466729.1:n.298-267T>C | |
| NM_000363.4:c.373-267T>C , LRG_432t1:c.373-267T>C | NP_000354.4:n.373-267T>C | |
| NM_000363.5:c.373-267T>C MANE Select | NP_000354.4:n.373-267T>C |