Linked Data
MyVariant Identifiers:
chr16:g.88798857G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88732449G>T , CM000678.2:g.88732449G>T | GRCh38 |
| NC_000016.9:g.88798857G>T , CM000678.1:g.88798857G>T | GRCh37 |
| NC_000016.8:g.87326358G>T | NCBI36 |
| NG_042229.1:g.57772C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.2877C>A (PIEZO1) MANE Select | ENSP00000301015.9:p.Ala959= | |
| ENST00000301015.13:c.2877C>A (PIEZO1) | ENSP00000301015.9:p.Ala959= | |
| NM_001142864.2:c.2877C>A (PIEZO1) | NP_001136336.2:p.Ala959= | |
| NM_001142864.3:c.2877C>A (PIEZO1) | NP_001136336.2:p.Ala959= | |
| NR_103774.1:n.269+1001G>T (HSALR1) | ||
| NM_001142864.4:c.2877C>A (PIEZO1) MANE Select | NP_001136336.2:p.Ala959= |