Linked Data
gnomAD v4:
11-61392433-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61392433G>T , CM000673.2:g.61392433G>T | GRCh38 |
| NC_000011.9:g.61159905G>T , CM000673.1:g.61159905G>T | GRCh37 |
| NC_000011.8:g.60916481G>T | NCBI36 |
| NG_032976.1:g.5074G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334888.9:c.-199G>T | ENSP00000334844.5:n.-199G>T | |
| ENST00000398979.7:c.-396G>T | ENSP00000381950.3:n.-396G>T | |
| ENST00000515837.6:c.-199G>T | ENSP00000440638.1:n.-199G>T | |
| NM_001173990.2:c.-199G>T | NP_001167461.1:n.-199G>T | |
| NM_001173991.2:c.-199G>T | NP_001167462.1:n.-199G>T | |
| NM_016499.5:c.-396G>T | NP_057583.2:n.-396G>T | |
| XM_005274039.3:c.-530G>T | XP_005274096.1:n.-530G>T | |
| NM_001330285.1:c.-396G>T | NP_001317214.1:n.-396G>T | |
| XM_005274039.4:c.-530G>T | XP_005274096.1:n.-530G>T |