Linked Data
gnomAD v4:
11-61392463-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61392463G>T , CM000673.2:g.61392463G>T | GRCh38 |
| NC_000011.9:g.61159935G>T , CM000673.1:g.61159935G>T | GRCh37 |
| NC_000011.8:g.60916511G>T | NCBI36 |
| NG_032976.1:g.5104G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334888.9:c.-169G>T | ENSP00000334844.5:n.-169G>T | |
| ENST00000398979.7:c.-366G>T | ENSP00000381950.3:n.-366G>T | |
| ENST00000515837.6:c.-169G>T | ENSP00000440638.1:n.-169G>T | |
| NM_001173990.2:c.-169G>T | NP_001167461.1:n.-169G>T | |
| NM_001173991.2:c.-169G>T | NP_001167462.1:n.-169G>T | |
| NM_016499.5:c.-366G>T | NP_057583.2:n.-366G>T | |
| XM_005274039.3:c.-500G>T | XP_005274096.1:n.-500G>T | |
| NM_001330285.1:c.-366G>T | NP_001317214.1:n.-366G>T | |
| XM_005274039.4:c.-500G>T | XP_005274096.1:n.-500G>T |