Linked Data
gnomAD v4:
4-55096482-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55096482T>C , CM000666.2:g.55096482T>C | GRCh38 |
| NC_000004.11:g.55962649T>C , CM000666.1:g.55962649T>C | GRCh37 |
| NC_000004.10:g.55657406T>C | NCBI36 |
| NG_012004.1:g.34114A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.2615-140A>G MANE Select | ENSP00000263923.4:n.2615-140A>G | |
| ENST00000647068.1:n.2628-140A>G | ||
| ENST00000263923.4:c.2615-140A>G | ENSP00000263923.4:n.2615-140A>G | |
| ENST00000509309.1:n.239A>G | ||
| NM_002253.2:c.2615-140A>G | NP_002244.1:n.2615-140A>G | |
| NM_002253.3:c.2615-140A>G | NP_002244.1:n.2615-140A>G | |
| NM_002253.4:c.2615-140A>G MANE Select | NP_002244.1:n.2615-140A>G |