Linked Data
dbSNP Id:
rs1344658357
gnomAD v3:
11-14893811-ATTC-A
gnomAD v4:
11-14893811-ATTC-A
MyVariant Identifiers:
chr11:g.14893812_14893814del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14893817_14893819del , CM000673.2:g.14893817_14893819del | GRCh38 |
| NC_000011.9:g.14915363_14915365del , CM000673.1:g.14915363_14915365del | GRCh37 |
| NC_000011.8:g.14871939_14871941del | NCBI36 |
| NG_007936.1:g.3392_3394del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011519898.1:c.-1570_-1568del | XP_011518200.1:n.-1570_-1568del | |
| XM_011519898.3:c.-1570_-1568del | XP_011518200.1:n.-1570_-1568del |