Linked Data
gnomAD v4:
4-55096541-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55096541A>G , CM000666.2:g.55096541A>G | GRCh38 |
| NC_000004.11:g.55962708A>G , CM000666.1:g.55962708A>G | GRCh37 |
| NC_000004.10:g.55657465A>G | NCBI36 |
| NG_012004.1:g.34055T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.2615-199T>C MANE Select | ENSP00000263923.4:n.2615-199T>C | |
| ENST00000647068.1:n.2628-199T>C | ||
| ENST00000263923.4:c.2615-199T>C | ENSP00000263923.4:n.2615-199T>C | |
| ENST00000509309.1:n.180T>C | ||
| NM_002253.2:c.2615-199T>C | NP_002244.1:n.2615-199T>C | |
| NM_002253.3:c.2615-199T>C | NP_002244.1:n.2615-199T>C | |
| NM_002253.4:c.2615-199T>C MANE Select | NP_002244.1:n.2615-199T>C |