HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88732588C>T , CM000678.2:g.88732588C>T | GRCh38 |
NC_000016.9:g.88798996C>T , CM000678.1:g.88798996C>T | GRCh37 |
NC_000016.8:g.87326497C>T | NCBI36 |
NG_042229.1:g.57633G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301015.14:c.2790+19G>A (PIEZO1) MANE Select | ENSP00000301015.9:n.2790+19G>A | |
ENST00000301015.13:c.2790+19G>A (PIEZO1) | ENSP00000301015.9:n.2790+19G>A | |
ENST00000490756.1:n.374+19G>A (PIEZO1) | ||
NM_001142864.2:c.2790+19G>A (PIEZO1) | NP_001136336.2:n.2790+19G>A | |
NM_001142864.3:c.2790+19G>A (PIEZO1) | NP_001136336.2:n.2790+19G>A | |
NR_103774.1:n.269+1140C>T (HSALR1) | ||
NM_001142864.4:c.2790+19G>A (PIEZO1) MANE Select | NP_001136336.2:n.2790+19G>A |