HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88733865A= , CM000678.2:g.88733865A= | GRCh38 |
NC_000016.9:g.88800273A= , CM000678.1:g.88800273A= | GRCh37 |
NC_000016.8:g.87327774A= | NCBI36 |
NG_042229.1:g.56356T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301015.14:c.2329+41T= (PIEZO1) MANE Select | ENSP00000301015.9:n.2329+41T= | |
ENST00000301015.13:c.2329+41T= (PIEZO1) | ENSP00000301015.9:n.2329+41T= | |
NM_001142864.2:c.2329+41T= (PIEZO1) | NP_001136336.2:n.2329+41T= | |
NM_001142864.3:c.2329+41T= (PIEZO1) | NP_001136336.2:n.2329+41T= | |
NR_103774.1:n.269+2417A= (HSALR1) | ||
NM_001142864.4:c.2329+41T= (PIEZO1) MANE Select | NP_001136336.2:n.2329+41T= |