Linked Data
gnomAD v4:
19-48965260-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48965260T>C , CM000681.2:g.48965260T>C | GRCh38 |
| NC_000019.9:g.49468517T>C , CM000681.1:g.49468517T>C | GRCh37 |
| NC_000019.8:g.54160329T>C | NCBI36 |
| NG_008152.1:g.4952T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_024451447.1:c.263T>C | XP_024307215.1:p.Leu88Pro |