Linked Data
gnomAD v4:
22-39244800-G-GT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.39244800_39244801insT , CM000684.2:g.39244800_39244801insT | GRCh38 |
| NC_000022.10:g.39640805_39640806insT , CM000684.1:g.39640805_39640806insT | GRCh37 |
| NC_000022.9:g.37970751_37970752insT | NCBI36 |
| NG_012111.1:g.5152_5153insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331163.11:c.-838_-837insA MANE Select | ENSP00000330382.6:n.-838_-837insA | |
| NM_002608.2:c.-838_-837insA | NP_002599.1:n.-838_-837insA | |
| NM_002608.3:c.-838_-837insA | NP_002599.1:n.-838_-837insA | |
| NM_002608.4:c.-838_-837insA MANE Select | NP_002599.1:n.-838_-837insA |