Linked Data
dbSNP Id:
rs1298547580
gnomAD v4:
1-149927914-CTT-C
MyVariant Identifiers:
chr1:g.149927915_149927916del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149927915_149927916del , CM000663.2:g.149927915_149927916del | GRCh38 |
| NC_000001.10:g.149899807_149899808del , CM000663.1:g.149899807_149899808del | GRCh37 |
| NC_000001.9:g.148166431_148166432del | NCBI36 |
| NG_032777.1:g.5337_5338del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-157_-156del | ENSP00000271628.8:n.-157_-156del | |
| NM_005850.4:c.-157_-156del | NP_005841.1:n.-157_-156del |