Linked Data
dbSNP Id:
rs758485588
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72225147_72225183del , CM000673.2:g.72225147_72225183del | GRCh38 |
| NC_000011.9:g.71936191_71936227del , CM000673.1:g.71936191_71936227del | GRCh37 |
| NC_000011.8:g.71613839_71613875del | NCBI36 |
| NG_023253.1:g.5310_5346del | |
| NG_023253.2:g.5310_5346del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298229.7:c.163_182+17del | ||
| ENST00000298229.6:c.163_182+17del | ||
| ENST00000541544.1:n.79_98+17del | ||
| NM_001567.3:c.163_182+17del | ||
| XM_005273978.3:c.163_182+17del | ||
| XM_005273979.3:c.163_182+17del | ||
| XM_011544999.1:c.163_182+17del | ||
| XM_011545000.1:c.163_182+17del | ||
| XM_005273979.4:c.163_182+17del | ||
| XM_011544999.2:c.163_182+17del | ||
| XM_024448501.1:c.163_182+17del | ||
| XM_024448502.1:c.163_182+17del | ||
| XM_024448503.1:c.42_61+17del | ||
| XM_024448504.1:c.163_182+17del | ||
| XM_024448505.1:c.163_182+17del | ||
| NM_001567.4:c.163_182+17del |