Linked Data
dbSNP Id:
rs1767440166
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49447598del , CM000668.2:g.49447598del | GRCh38 |
| NC_000006.11:g.49415311del , CM000668.1:g.49415311del | GRCh37 |
| NC_000006.10:g.49523270del | NCBI36 |
| NG_007100.1:g.20542del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.1560+72del MANE Select | ENSP00000274813.3:n.1560+72del | |
| ENST00000274813.3:c.1560+72del | ENSP00000274813.3:n.1560+72del | |
| NM_000255.3:c.1560+72del | NP_000246.2:n.1560+72del | |
| XM_005249143.2:c.1560+72del | XP_005249200.1:n.1560+72del | |
| XM_005249143.3:c.1560+72del | XP_005249200.1:n.1560+72del | |
| NM_000255.4:c.1560+72del MANE Select | NP_000246.2:n.1560+72del |