Linked Data
dbSNP Id:
rs2126355964
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1415342_1415344del , CM000667.2:g.1415342_1415344del | GRCh38 |
| NC_000005.9:g.1415457_1415459del , CM000667.1:g.1415457_1415459del | GRCh37 |
| NC_000005.8:g.1468457_1468459del | NCBI36 |
| NG_015885.1:g.35085_35087del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1032-529_1032-527del MANE Select | ENSP00000270349.9:n.1032-529_1032-527del | |
| ENST00000270349.11:c.1032-529_1032-527del | ENSP00000270349.9:n.1032-529_1032-527del | |
| ENST00000511750.1:n.482-529_482-527del | ||
| NM_001044.4:c.1032-529_1032-527del | NP_001035.1:n.1032-529_1032-527del | |
| NM_001044.5:c.1032-529_1032-527del MANE Select | NP_001035.1:n.1032-529_1032-527del |