Linked Data
gnomAD v4:
11-61392359-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61392359C>A , CM000673.2:g.61392359C>A | GRCh38 |
| NC_000011.9:g.61159831C>A , CM000673.1:g.61159831C>A | GRCh37 |
| NC_000011.8:g.60916407C>A | NCBI36 |
| NG_032976.1:g.5000C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515837.6:c.-273C>A | ENSP00000440638.1:n.-273C>A | |
| XM_005274039.3:c.-604C>A | XP_005274096.1:n.-604C>A | |
| XM_005274039.4:c.-604C>A | XP_005274096.1:n.-604C>A |