Linked Data
gnomAD v4:
12-52433766-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52433766T>G , CM000674.2:g.52433766T>G | GRCh38 |
| NC_000012.11:g.52827550T>G , CM000674.1:g.52827550T>G | GRCh37 |
| NC_000012.10:g.51113817T>G | NCBI36 |
| NG_008403.1:g.5561A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252245.6:c.498+41A>C MANE Select | ENSP00000252245.5:n.498+41A>C | |
| ENST00000252245.5:c.498+41A>C | ENSP00000252245.5:n.498+41A>C | |
| NM_004693.2:c.498+41A>C | NP_004684.2:n.498+41A>C | |
| NM_004693.3:c.498+41A>C MANE Select | NP_004684.2:n.498+41A>C |