Linked Data
dbSNP Id:
rs796179127
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869089_240869090delinsAC , CM000664.2:g.240869089_240869090delinsAC | GRCh38 |
| NC_000002.11:g.241808506_241808507delinsAC , CM000664.1:g.241808506_241808507delinsAC | GRCh37 |
| NC_000002.10:g.241457179_241457180delinsAC | NCBI36 |
| NG_008005.1:g.5345_5346delinsAC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.165+59_165+60delinsAC MANE Select | ENSP00000302620.3:n.165+59_165+60delinsAC... | |
| ENST00000307503.3:c.165+59_165+60delinsAC | ENSP00000302620.3:n.165+59_165+60delinsAC... | |
| ENST00000472436.1:n.185+59_185+60delinsAC | ||
| NM_000030.2:c.165+59_165+60delinsAC | NP_000021.1:n.165+59_165+60delinsAC | |
| XR_924060.1:n.405+1143_405+1144delinsGT | ||
| NM_000030.3:c.165+59_165+60delinsAC MANE Select | NP_000021.1:n.165+59_165+60delinsAC |