Linked Data
gnomAD v4:
19-2275193-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2275193C>T , CM000681.2:g.2275193C>T | GRCh38 |
| NC_000019.9:g.2275192C>T , CM000681.1:g.2275192C>T | GRCh37 |
| NC_000019.8:g.2226192C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342063.5:c.*487G>A MANE Select | ENSP00000345102.3:n.*487G>A | |
| ENST00000342063.4:c.*487G>A | ENSP00000345102.3:n.*487G>A | |
| ENST00000621615.1:c.146+5449C>T | ENSP00000481965.1:n.146+5449C>T | |
| NM_198532.2:c.*487G>A | NP_940934.1:n.*487G>A | |
| NM_198532.3:c.*487G>A MANE Select | NP_940934.1:n.*487G>A |