Linked Data
gnomAD v4:
4-88008441-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88008441T>C , CM000666.2:g.88008441T>C | GRCh38 |
| NC_000004.11:g.88929593T>C , CM000666.1:g.88929593T>C | GRCh37 |
| NC_000004.10:g.89148617T>C | NCBI36 |
| NG_008604.1:g.5774T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.595+113T>C MANE Select | ENSP00000237596.2:n.595+113T>C | |
| ENST00000237596.6:c.595+113T>C | ENSP00000237596.2:n.595+113T>C | |
| ENST00000506727.1:n.97+113T>C | ||
| NM_000297.3:c.595+113T>C | NP_000288.1:n.595+113T>C | |
| XM_011532028.1:c.595+113T>C | XP_011530330.1:n.595+113T>C | |
| XR_244632.2:n.690+113T>C | ||
| NR_156488.1:n.682+113T>C | ||
| XM_011532028.2:c.595+113T>C | XP_011530330.1:n.595+113T>C | |
| NM_000297.4:c.595+113T>C MANE Select | NP_000288.1:n.595+113T>C | |
| NR_156488.2:n.694+113T>C |