Linked Data
gnomAD v2:
16-67470907-G-A
MyVariant Identifiers:
chr16:g.67470907_67470908delinsAC (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67437004G>A , CM000678.2:g.67437004G>A | GRCh38 |
| NC_000016.9:g.67470907G>A , CM000678.1:g.67470907G>A | GRCh37 |
| NC_000016.8:g.66028408G>A | NCBI36 |
| NG_011482.1:g.49183C>T | |
| NG_016549.1:g.10872G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.*1G>A MANE Select | ENSP00000316786.5:n.*1G>A | |
| ENST00000326152.5:c.*1G>A | ENSP00000316786.5:n.*1G>A | |
| NM_000196.3:c.*1G>A | NP_000187.3:n.*1G>A | |
| NM_000196.4:c.*1G>A MANE Select | NP_000187.3:n.*1G>A |